The following data is part of a premarket notification filed by Keeler Instruments, Inc. with the FDA for Vickers Ergomatic Micros Instr-long R Or L Handed.
Device ID | K853180 |
510k Number | K853180 |
Device Name: | VICKERS ERGOMATIC MICROS INSTR-LONG R OR L HANDED |
Classification | Instrument, Microsurgical |
Applicant | KEELER INSTRUMENTS, INC. 456 PKWY. Broomall, PA 19008 |
Contact | Van Arsdale |
Correspondent | Van Arsdale KEELER INSTRUMENTS, INC. 456 PKWY. Broomall, PA 19008 |
Product Code | GZX |
CFR Regulation Number | 882.4525 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-07-30 |
Decision Date | 1985-10-28 |