The following data is part of a premarket notification filed by Busse Hospital Disposables, Inc. with the FDA for Busse Surgical Drapes Iv.
Device ID | K093909 |
510k Number | K093909 |
Device Name: | BUSSE SURGICAL DRAPES IV |
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 | 2009-12-22 |
Decision Date | 2010-05-06 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00849233013902 | K093909 | 000 |