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

GRASPING FORCEP, 1.7MM

K Number: K871926 · Decision Jun 9, 1987
Classifications
1
FEI Numbers
444
Registration Numbers
445
Same Product Code
103
Applicant Total
29
Review Days
22

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Basic Information

Device Name
GRASPING FORCEP, 1.7MM
K Number
K871926
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
May 18, 1987
Decision Date
June 9, 1987
Product Code
GEN
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
GEN Forceps, General & Plastic Surgery

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GEN), 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
K873504 CUP BIOPSY FORCEPS, RIGHT
K872533 THE CART
K873501 SCISSOR, LEFT
K873502 SCISSOR, RIGHT
K873512 SERRATED GRASPING FORCEPS, RIGHT
Search all 29 clearances from Arthropedics, Inc. →