Keeler Spectra Indirect Ophthalmoscope
FDA 510(k) K970029 · Keeler Instruments, Inc.
510(k) numberK970029
Submission
- Device name
- Keeler Spectra Indirect Ophthalmoscope
- Applicant
- Keeler Instruments, Inc.
Broomall, PA, US - Received
- January 3, 1997
- Decision date
- April 2, 1997
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- HLJ – Ophthalmoscope, Battery-Powered
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 886.1570
- Specialty
- Ophthalmic
Other 510(k)s with product code HLJ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K142486 | Heine Beta 200, Heine Beta 200 S, Heine K 180HLJ · Abbreviated | Heine Optotechnik GmbH & Co. KG | 05/18/2015SE |
| K142837 | Heine Sigma 250 & Heine Sigma 250 M2HLJ · Abbreviated | Heine Optotechnik GmbH & Co. KG | 01/29/2015SE |
| K131959 | Heine Mini 3000(R) OphthalmoscopeHLJ · Abbreviated | Heine Optotechnik GmbH & Co. KG | 03/07/2014SE |
| K131961 | Heine Beta 200(R) OphthalmoscopeHLJ · Abbreviated | Heine Optotechnik GmbH & Co. KG | 12/04/2013SE |
| K131719 | Ophthalmoscopes Diagnostic Instrument KitsHLJ · Traditional | Medical Devices (Pvt) , Ltd. | 10/30/2013SE |
| K123587 | Heine Mini 3000 LED OphthalmoscopeHLJ · Abbreviated | Heine Optotechnik GmbH & Co. KG | 03/22/2013SE |
| K093495 | Otoscope and Ophthalmoscope Diagnostic Instrument KitsHLJ · Traditional | American Diagnostic Corp. | 11/19/2010SE |
| K070270 | Piccolight E50,PICCOLIGHT E56,EUROLIGHT E10, Eurolight E30, and Eurolight E36HLJ · Traditional | Kirchner & Wilhelm GmbH + Co.Kg | 11/05/2007SE |
| K052599 | 66 Vision Tech Ophthalmoscope, Models YZ6E, YZ6F, YZ6G, YZ11, YZ11C, YZ11D, YZ25AHLJ · Traditional | Suzhou 66 Vision Tech Co., Ltd. | 11/07/2006SE |
| K061278 | Optyse OphthalmoscopeHLJ · Abbreviated | Ophthalmos , Ltd. | 05/16/2006SE |
More from Ophthalmos , Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K181143 | Keeler TonoCare TonometerHKX · Traditional | 02/08/2019SE |
| K112093 | Cryomatic Cryo Console, Disposable Cryo Probe, Disposable Probe AdapterHRN · Special | 12/08/2011SE |
| K093298 | Pulsair Intellipuff, Pulsair Desktop Model 2414-P-2001, 2417-P-2000HKX · Traditional | 12/10/2010SE |
| K100500 | PSL Classic Slit LampHJO · Traditional | 03/09/2010SE |
| K062412 | CryomaticHRN · Traditional | 11/06/2006SE |
| K060822 | Vantage Indirect OphthalmoscopeHLI · Special | 05/23/2006SE |
| K032087 | Keeler Wide Angle Ophthalmoscope Model 1130-P-5004HLJ · Traditional | 11/26/2003SE |
| K992954 | Keeler Cryo Master & ProbesHRN · Traditional | 12/21/1999SE |
| K990257 | Keeler Pulsair 3000 Non Contact TonometerHKX · Traditional | 03/25/1999SE |
| K973064 | Keeler Tearscope-PlusHJO · Traditional | 04/07/1998SE |
Questions and answers
When was Keeler Spectra Indirect Ophthalmoscope cleared by the FDA?
Keeler Spectra Indirect Ophthalmoscope (K970029) received a 510(k) decision of Substantially Equivalent on April 2, 1997, 89 days after the submission was received.
What is the product code of K970029?
The FDA product code is HLJ – Ophthalmoscope, Battery-Powered, a Class II (moderate risk) device regulated under 21 CFR 886.1570.