FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CUP BIOPSY FORCEPS, RIGHT

K Number: K873504 · Decision Nov 2, 1987
Classifications
1
FEI Numbers
658
Registration Numbers
658
Same Product Code
72
Applicant Total
29
Review Days
63

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Basic Information

Device Name
CUP BIOPSY FORCEPS, RIGHT
K Number
K873504
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Arthropedics, Inc.
Date Received
August 31, 1987
Decision Date
November 2, 1987
Product Code
HTD
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
HTD Forceps

Similar 510(k) Clearances

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

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Other Clearances by Arthropedics, Inc.

K Number Device Name
K873619 ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS)
K873655 MONOPOLAR CAUTERY RETROGADE TIP #TM-1703
K873653 MONOPOLAR CAUTERY BLADE TIP #TM-1701
K873654 MONOPOLAR CAUTERY CONICAL TIP #TM-1702
K873387 VIDEO ARTHROSCOPE, 1.7MM X 55 MM
K872533 THE CART
K873501 SCISSOR, LEFT
K873502 SCISSOR, RIGHT
K873512 SERRATED GRASPING FORCEPS, RIGHT
K873710 MAGNETIC RETRIEVER, 1.7MM W/LUER FITTING TM-1350
Search all 29 clearances from Arthropedics, Inc. →