Atlas FDA

CUP BIOPSY FORCEPS, LEFT

FDA 510(k) clearance K873503 · decided 1987-11-02

Clearance details

K-number
K873503
Device name
CUP BIOPSY FORCEPS, LEFT
Applicant
Arthropedics, Inc.
Decision
Substantially Equivalent
Date received
1987-08-31
Decision date
1987-11-02
Days to decision
63 days
Clearance type
Traditional
Product code
HTD
Device class
1
Regulation number
878.4800
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Wallington, NJ, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
THE NEEDLE CATCHER (K051281)E.D.Medical , Ltd.2005-09-08
SEMKIN BIPOLAR FORCEP (K974594)Titan Mfg., Inc.1998-06-24
CUSHING BAYONET, INSULATED BIPOLAR FORCEP (K974595)Titan Mfg., Inc.1998-06-24
SEMKIN INSULATED BIPOLAR FORCEP (K974593)Titan Mfg., Inc.1998-06-24
MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPS (K913964)Marlo Surgical Technology1991-10-23
CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPS (K911180)Northgate Technologies, Inc.1991-03-29
TIK EXTRAKTOR (K895212)Instruments of Sweden, Inc.1989-09-27
HEMORRHOIDAL FORCEPS (K890373)Kinetic Medical Products1989-02-03
GALL STONE FORCEPS (K890369)Kinetic Medical Products1989-02-03
TUBING CLAMP FORCEPS (K890244)Kinetic Medical Products1989-01-27
BONE CUTTING FORCEPS, SINGLE-ACTION (K890258)Kinetic Medical Products1989-01-27
LUNG FORCEPS (K890262)Kinetic Medical Products1989-01-27

Recalls involving this device

No recalls on record reference this clearance.