The following data is part of a premarket notification filed by Busse Hospital Disposables, Inc. with the FDA for Busse Surgical Drape.
| Device ID | K082297 |
| 510k Number | K082297 |
| Device Name: | BUSSE SURGICAL DRAPE |
| Classification | Drape, Surgical |
| Applicant | BUSSE HOSPITAL DISPOSABLES, INC. 75 ARKAY DR. Hauppauge, NY 11788 |
| Contact | Muhamad Ansari |
| Correspondent | Muhamad Ansari BUSSE HOSPITAL DISPOSABLES, INC. 75 ARKAY DR. Hauppauge, NY 11788 |
| Product Code | KKX |
| CFR Regulation Number | 878.4370 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-08-12 |
| Decision Date | 2008-12-09 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00849233013476 | K082297 | 000 |
| 00849233013445 | K082297 | 000 |