The following data is part of a premarket notification filed by Acuderm, Inc. with the FDA for Acu-evac.
Device ID | K930043 |
510k Number | K930043 |
Device Name: | ACU-EVAC |
Classification | Apparatus, Exhaust, Surgical |
Applicant | ACUDERM, INC. 5370 N.W. 35TH TERRACE Ft. Lauderdale, FL 33309 |
Contact | Charles R Yeh |
Correspondent | Charles R Yeh ACUDERM, INC. 5370 N.W. 35TH TERRACE Ft. Lauderdale, FL 33309 |
Product Code | FYD |
CFR Regulation Number | 878.5070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-01-05 |
Decision Date | 1994-02-09 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
10814105020507 | K930043 | 000 |
00814105020579 | K930043 | 000 |
00814105020562 | K930043 | 000 |
00814105020555 | K930043 | 000 |
00814105020548 | K930043 | 000 |
00814105020531 | K930043 | 000 |
00814105020524 | K930043 | 000 |
00814105020517 | K930043 | 000 |
00814105020487 | K930043 | 000 |
00814105020586 | K930043 | 000 |
00814105021668 | K930043 | 000 |
10814105020392 | K930043 | 000 |
10814105020491 | K930043 | 000 |
10814105020460 | K930043 | 000 |
10814105020453 | K930043 | 000 |
10814105020446 | K930043 | 000 |
10814105020439 | K930043 | 000 |
10814105020422 | K930043 | 000 |
10814105020415 | K930043 | 000 |
10814105020408 | K930043 | 000 |
00814105020470 | K930043 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() ACU-EVAC 74420739 1831240 Live/Registered |
Acuderm Inc. 1993-08-05 |