The following data is part of a premarket notification filed by Wilson Greatbatch Technologies, Inc. with the FDA for Greatbatch Scientific Mr Compatible Sinuscope.
Device ID | K971375 |
510k Number | K971375 |
Device Name: | GREATBATCH SCIENTIFIC MR COMPATIBLE SINUSCOPE |
Classification | Nasopharyngoscope (flexible Or Rigid) |
Applicant | WILSON GREATBATCH TECHNOLOGIES, INC. 4100 BARTON RD. Clarence, NY 14031 |
Contact | Gary J Sfeir |
Correspondent | Gary J Sfeir WILSON GREATBATCH TECHNOLOGIES, INC. 4100 BARTON RD. Clarence, NY 14031 |
Product Code | EOB |
CFR Regulation Number | 874.4760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-04-14 |
Decision Date | 1997-10-31 |
Summary: | summary |