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FDA 510(k)

CUP BIOPSY FORCEPS, RIGHT

K-Number: K873504 · 1987-11-02

ApplicantArthropedics, Inc.
Decision Date1987-11-02
Product CodeHTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CUP BIOPSY FORCEPS, RIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Arthropedics, Inc.. It received FDA 510(k) clearance on 1987-11-02 under 510(k) number K873504. The device is classified under product code HTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUP BIOPSY FORCEPS, RIGHT?

CUP BIOPSY FORCEPS, RIGHT is a medical device that received FDA 510(k) clearance on 1987-11-02. The listed applicant is Arthropedics, Inc.. The 510(k) number is K873504.

When did CUP BIOPSY FORCEPS, RIGHT receive FDA 510(k) clearance?

CUP BIOPSY FORCEPS, RIGHT received FDA 510(k) clearance on 1987-11-02, under 510(k) number K873504.

Who is the listed applicant for CUP BIOPSY FORCEPS, RIGHT?

The FDA 510(k) record lists Arthropedics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CUP BIOPSY FORCEPS, RIGHT?

The FDA product code for CUP BIOPSY FORCEPS, RIGHT is HTD.

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Other records listing Arthropedics, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K873619ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS)K873653MONOPOLAR CAUTERY BLADE TIP #TM-1701K873654MONOPOLAR CAUTERY CONICAL TIP #TM-1702K873655MONOPOLAR CAUTERY RETROGADE TIP #TM-1703K873387VIDEO ARTHROSCOPE, 1.7MM X 55 MMK873711RETROGRADE KNIFE, DISPOSABLE #TM-1613

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Related Devices (Code: HTD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K051281THE NEEDLE CATCHERE.D.Medical , Ltd.K974595CUSHING BAYONET, INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K974594SEMKIN BIPOLAR FORCEPTitan Mfg., Inc.K974593SEMKIN INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K913964MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPSMarlo Surgical TechnologyK911180CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPSNorthgate Technologies, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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