The following data is part of a premarket notification filed by Devmed Corp. with the FDA for Devmed Lens Wash Sheath.
Device ID | K925669 |
510k Number | K925669 |
Device Name: | DEVMED LENS WASH SHEATH |
Classification | Laparoscope, General & Plastic Surgery |
Applicant | DEVMED CORP. P.O. BOX 30716 Palm Beach Gardens, FL 33420 |
Contact | Greg D Wiita |
Correspondent | Greg D Wiita DEVMED CORP. P.O. BOX 30716 Palm Beach Gardens, FL 33420 |
Product Code | GCJ |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-11-10 |
Decision Date | 1993-02-23 |