Modified Site Peristaltic Footswitch
FDA 510(k) K905620 · Site Microsurgical Systems, Inc.
510(k) numberK905620
Submission
- Device name
- Modified Site Peristaltic Footswitch
- Applicant
- Site Microsurgical Systems, Inc.
Horsham, PA, US - Received
- December 14, 1990
- Decision date
- February 27, 1991
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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More from Guilin Woodpecker Medical Instrument Co., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K925828 | Modified Site TXR SystemsHQC · Traditional | 02/16/1994SE |
| K925921 | Modified Site Disposable Diaphragm CassetteKYG · Traditional | 12/06/1993SE |
| K931866 | Site's CD II Phacoemulsification HandpieceHQC · Traditional | 11/12/1993SE |
| K921135 | Iolab Power I.V. PoleHQC · Traditional | 06/03/1992SE |
| K920582 | 180 Tip, 1/A Handpiece .3MM End Opening for Opht.HQE · Traditional | 05/08/1992SE |
| K912902 | Phacoemulsification System for Ophthalmic UseHQC · Traditional | 12/17/1991SE |
| K912739 | Site 90 Tip, I/A Handpiece .3MM Side Open/Opth UseHQC · Traditional | 08/28/1991SE |
| K910980 | Site 20 Gauge Reusable Fiber Optic CableHJO · Traditional | 05/22/1991SE |
| K904183 | Site Phacoemulsification HandpieceHQC · Traditional | 12/05/1990SE |
| K904151 | Site 19 Gauge Ultrasonic I/A Phaco NeedleHQC · Traditional | 12/05/1990SE |
Questions and answers
When was Modified Site Peristaltic Footswitch cleared by the FDA?
Modified Site Peristaltic Footswitch (K905620) received a 510(k) decision of Substantially Equivalent on February 27, 1991, 75 days after the submission was received.
What is the product code of K905620?
The FDA product code is EBW – Controller, Foot, Handpiece And Cord, a Class I (low risk) device regulated under 21 CFR 872.4200.