The following data is part of a premarket notification filed by Grieshaber & Co. with the FDA for Grieshaber Three Function Manipulator.
Device ID | K914586 |
510k Number | K914586 |
Device Name: | GRIESHABER THREE FUNCTION MANIPULATOR |
Classification | Source, Carrier, Fiberoptic Light |
Applicant | GRIESHABER & CO. 3000 CABOT BLVD. WEST P.O. BOX 1099 Langhorne, PA 19047 |
Contact | John E Richmond |
Correspondent | John E Richmond GRIESHABER & CO. 3000 CABOT BLVD. WEST P.O. BOX 1099 Langhorne, PA 19047 |
Product Code | EQH |
CFR Regulation Number | 874.4350 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-10-16 |
Decision Date | 1992-01-03 |