CUP BIOPSY FORCEPS, CURVED DOWN

Forceps

ARTHROPEDICS, INC.

The following data is part of a premarket notification filed by Arthropedics, Inc. with the FDA for Cup Biopsy Forceps, Curved Down.

Pre-market Notification Details

Device IDK873505
510k NumberK873505
Device Name:CUP BIOPSY FORCEPS, CURVED DOWN
ClassificationForceps
Applicant ARTHROPEDICS, INC. 111 LESTER ST. Wallington,  NJ  07057
ContactJerry Procopio
CorrespondentJerry Procopio
ARTHROPEDICS, INC. 111 LESTER ST. Wallington,  NJ  07057
Product CodeHTD  
CFR Regulation Number878.4800 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1987-08-31
Decision Date1987-11-02

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