The following data is part of a premarket notification filed by Pilling Co. with the FDA for Triangular Jaw Microlaryngeal Forceps.
Device ID | K925370 |
510k Number | K925370 |
Device Name: | TRIANGULAR JAW MICROLARYNGEAL FORCEPS |
Classification | Material, Impression |
Applicant | PILLING CO. 420 DELAWARE DR. Fort Washington, PA 19034 |
Contact | Richard G Jones |
Correspondent | Richard G Jones PILLING CO. 420 DELAWARE DR. Fort Washington, PA 19034 |
Product Code | ELW |
CFR Regulation Number | 872.3660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-10-23 |
Decision Date | 1993-03-18 |