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FDA 510(k)

GRASPING FORCEP, 1.7MM

K-Number: K871926 · 1987-06-09

ApplicantArthropedics, Inc.
Decision Date1987-06-09
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GRASPING FORCEP, 1.7MM is the device name listed in this FDA 510(k) record. The listed applicant is Arthropedics, Inc.. It received FDA 510(k) clearance on 1987-06-09 under 510(k) number K871926. The device is classified under product code GEN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRASPING FORCEP, 1.7MM?

GRASPING FORCEP, 1.7MM is a medical device that received FDA 510(k) clearance on 1987-06-09. The listed applicant is Arthropedics, Inc.. The 510(k) number is K871926.

When did GRASPING FORCEP, 1.7MM receive FDA 510(k) clearance?

GRASPING FORCEP, 1.7MM received FDA 510(k) clearance on 1987-06-09, under 510(k) number K871926.

Who is the listed applicant for GRASPING FORCEP, 1.7MM?

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 GRASPING FORCEP, 1.7MM?

The FDA product code for GRASPING FORCEP, 1.7MM is GEN.

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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: GEN)

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.

K031828NATURALASE LP ND:YAG LASERFocus Medical, LLCK953962FORCEPSBiopsys Medical, Inc.K932385SUTURE REMOVING FORCEPSRocket of London, Ltd.K904723FORCEPSMinto Research & Development, Inc.K911159PALPATION PROBENorthgate Technologies, Inc.K900952GS-1200 GRASPING/EXTRACTING FORCEP, 10MMSolos Endoscopy, 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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