The following data is part of a premarket notification filed by Midmark Corp. with the FDA for 712 Plastic Surgery Table & Accesories.
Device ID | K915141 |
510k Number | K915141 |
Device Name: | 712 PLASTIC SURGERY TABLE & ACCESORIES |
Classification | Table, Operating-room, Ac-powered |
Applicant | MIDMARK CORP. 60 VISTA DR. P.O. BOX 286 Versailles, OH 45380 |
Contact | John Oldiges |
Correspondent | John Oldiges MIDMARK CORP. 60 VISTA DR. P.O. BOX 286 Versailles, OH 45380 |
Product Code | FQO |
CFR Regulation Number | 878.4960 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-11-13 |
Decision Date | 1992-01-09 |