Stockings, RVS TM
FDA 510(k) K770466 · Parke-Davis Co.
510(k) numberK770466
Submission
- Device name
- Stockings, RVS TM
- Applicant
- Parke-Davis Co.
Mchenry, IL, US - Received
- March 10, 1977
- Decision date
- March 28, 1977
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- EQL – Laryngostroboscope
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 874.4750
- Specialty
- Ear, Nose, Throat
Other 510(k)s with product code EQL
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K984521 | Riwo Drive System 2302 with Generator, Small Motor Handles, 8563.111, 8563.351EQL · Traditional | Richard Wolf Medical Instruments Corp. | 03/17/1999SE |
| K921285 | 9105 Rigid Telescopic EndoscopeEQL · Traditional | Kay Elemetrics Corp. | 05/28/1992SE |
| K921184 | RLS 9100 Rhino-Laryngeal StroboscopeEQL · Traditional | Kay Elemetrics Corp. | 05/28/1992SE |
| K884933 | Endostroboscope IVEQL · Traditional | Jedmed Instrument Co. | 02/15/1989SE |
| K842090 | Rhino-Larynx Stroboscope Type 4914EQL · Traditional | Bruel & Kjaer Industri A/S | 07/18/1984SE |
| K822523 | LaryngostroboscopeEQL · Traditional | Kelleher Corp. | 09/09/1982SE |
| K801866 | Pentax Laryngo-Stroboscope Model LS-1AEQL · Traditional | Pentax Precision Instrument Corp. | 09/16/1980SE |
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| 510(k) | Device | Decision |
|---|---|---|
| K861725 | Intracath Intravenous Catheter Placement UnitFOZ · Traditional | 12/04/1986SE |
| K862119 | Deseret Flo-Thru Injectate Temperature SensorDYG · Traditional | 08/29/1986SE |
| K855120 | Ati Disposable Biological Test PackFRC · Traditional | 06/18/1986SE |
| K860570 | Angio-Flo Continuous Arterial Cath Flush DeviceKRA · Traditional | 03/31/1986SE |
| K860290 | Viapic Central Line CatheterFOZ · Traditional | 03/18/1986SE |
| K852192 | Disposable Steam Biological Test PackFRC · Traditional | 11/01/1985SE |
| K841967 | Deseret Thermodilution Cardiac OutputDXG · Traditional | 08/19/1985SE |
| K851327 | Deseret Arterial CatheterFOZ · Traditional | 06/14/1985SE |
| K852078 | Spectrum(Tentative)FOZ · Traditional | 06/07/1985SE |
| K844840 | Deseret Introducer SetDYB · Traditional | 05/16/1985SE |
Questions and answers
When was Stockings, RVS TM cleared by the FDA?
Stockings, RVS TM (K770466) received a 510(k) decision of Substantially Equivalent on March 28, 1977, 18 days after the submission was received.
What is the product code of K770466?
The FDA product code is EQL – Laryngostroboscope, a Class I (low risk) device regulated under 21 CFR 874.4750.