The following data is part of a premarket notification filed by Advance Medical Designs, Inc. with the FDA for Patient Drape, Surgical.
Device ID | K003670 |
510k Number | K003670 |
Device Name: | PATIENT DRAPE, SURGICAL |
Classification | Drape, Surgical |
Applicant | ADVANCE MEDICAL DESIGNS, INC. 1241 ATLANTA INDUSTRIAL DR. Marietta, GA 30066 |
Contact | Bill Gill |
Correspondent | Bill Gill ADVANCE MEDICAL DESIGNS, INC. 1241 ATLANTA INDUSTRIAL DR. Marietta, GA 30066 |
Product Code | KKX |
CFR Regulation Number | 878.4370 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-11-28 |
Decision Date | 2001-01-26 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
10848340010498 | K003670 | 000 |