1205 Betaplate Liquid Scintillation Counter
FDA 510(k) K874094 · Lkb Instruments, Inc.
510(k) numberK874094
Submission
- Device name
- 1205 Betaplate Liquid Scintillation Counter
- Applicant
- Lkb Instruments, Inc.
Gaithersburg, MD, US - Received
- September 30, 1987
- Decision date
- November 4, 1987
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- JJJ – Counter (Beta, Gamma) For Clinical Use
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 862.2320
- Specialty
- Clinical Chemistry
Other 510(k)s with product code JJJ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K962762 | Sequential Sample Multi-Photon DetectorJJJ · Traditional | Biotraces, Inc. | 08/16/1996SE |
| K946387 | Capra (Caprac-R) Wipetest and Well CounterJJJ · Traditional | Capintec, Inc. | 03/30/1995SE |
| K920559 | Abbott Vertex AnalyzerJJJ · Traditional | Abbott Laboratories | 03/19/1992SE |
| K900087 | Genesys 6000 Gamma CounterJJJ · Traditional | Laboratory Technologies, Inc. | 07/19/1990SE |
| K896202 | MATRIX(TM)-96JJJ · Traditional | Canberra Industries, Inc. | 01/02/1990SE |
| K894902 | SourcererJJJ · Traditional | Oakfield Instruments, Ltd. | 10/17/1989SE |
| K884091 | SourcererJJJ · Traditional | John Caunt Scientific , Ltd. | 02/02/1989SE |
| K884269 | Sample Identification Station Model 38010JJJ · Traditional | Icn Micromedic Systems | 01/09/1989SE |
| K872430 | Iso-Data 500 Series Gamma CounterJJJ · Traditional | Iso-Data, Inc. | 08/21/1987SE |
| K872429 | Iso-Data 100 Series Gamma CounterJJJ · Traditional | Iso-Data, Inc. | 08/21/1987SE |
More from Iso-Data, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K872955 | Delfia(Tm) Ferritin KitJMG · Traditional | 08/21/1987SE |
| K871303 | Delfia(Tm) Thyroxine (T4) KitCDX · Traditional | 06/17/1987SE |
| K871599 | Delfia(Tm) Hige KitDHB · Traditional | 06/12/1987SE |
| K871644 | Delfia (TM) HTSH KitJLW · Traditional | 05/12/1987SE |
| K864452 | Delfia(Tm) Triiodothyronine (T3) KitCDP · Traditional | 02/02/1987SE |
| K864733 | LKB 2260 MacrotomeIDO · Traditional | 01/05/1987SE |
| K862848 | LKB Ultrobact (TM) Pneumococcus Kit; 2321-110GWC · Traditional | 12/18/1986SE |
| K863422 | Delfia(Tm) Cortisol KitJFT · Traditional | 09/26/1986SE |
| K862044 | Delfia (TM) HCG KitJHJ · Traditional | 07/11/1986SE |
| K861195 | Delfia DigoxinKXT · Traditional | 07/11/1986SE |
Questions and answers
When was 1205 Betaplate Liquid Scintillation Counter cleared by the FDA?
1205 Betaplate Liquid Scintillation Counter (K874094) received a 510(k) decision of Substantially Equivalent on November 4, 1987, 35 days after the submission was received.
What is the product code of K874094?
The FDA product code is JJJ – Counter (Beta, Gamma) For Clinical Use, a Class I (low risk) device regulated under 21 CFR 862.2320.