FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CANNULATED BIOPSY FORCEPS

K Number: K926430 · Decision Mar 26, 1993
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
238
Applicant Total
33
Review Days
93

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Basic Information

Device Name
CANNULATED BIOPSY FORCEPS
K Number
K926430
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4680
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Thomasville Medical Assoc.
Date Received
December 23, 1992
Decision Date
March 26, 1993
Product Code
EOQ
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EOQ Bronchoscope (Flexible Or Rigid)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EOQ), ordered by most recent decision date.

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Other Clearances by Thomasville Medical Assoc.

K Number Device Name
K926429 VAGINAL SPECULA: CUSCO, GUTTMAN, INFANT
K926531 HYSTERECTOMY FORCEPS
K926527 ROTO FIT BIOPSY FORCEPS
K926535 GOMCO CIRCUMCISION CLAMP
K926533 Z-CLAMP FORCEPS
K926540 SOPHER AND BIERER OVUM FORCEPS
K926532 ENDO CERVICAL CURETTE
K926536 DISPOSABLE PLASTIC VAGINAL SPECULA
K930030 SUCTION TUBES: HOUSE, BARON
K926484 CORSON MYOMA GRASPING FORCEPS
Search all 33 clearances from Thomasville Medical Assoc. →