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FDA 510(k)

MICRINS FORCEPS 2010

K-Number: K872991 · 1987-08-17

ApplicantMicrins Surgical, Inc.
Decision Date1987-08-17
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICRINS FORCEPS 2010 is the device name listed in this FDA 510(k) record. The listed applicant is Micrins Surgical, Inc.. It received FDA 510(k) clearance on 1987-08-17 under 510(k) number K872991. 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 MICRINS FORCEPS 2010?

MICRINS FORCEPS 2010 is a medical device that received FDA 510(k) clearance on 1987-08-17. The listed applicant is Micrins Surgical, Inc.. The 510(k) number is K872991.

When did MICRINS FORCEPS 2010 receive FDA 510(k) clearance?

MICRINS FORCEPS 2010 received FDA 510(k) clearance on 1987-08-17, under 510(k) number K872991.

Who is the listed applicant for MICRINS FORCEPS 2010?

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

What is the FDA product code for MICRINS FORCEPS 2010?

The FDA product code for MICRINS FORCEPS 2010 is GEN.

Related Clinical Trials

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.

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Other records listing Micrins Surgical, 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.

K993970MICRINS MICROSURGICAL SUTUREK982278MICRINS MICRO ANASTOMOSIS CLAMPK933310MICRINS CONTRAST BACKGROUND MATERIALK872989MICRINS NEEDLE HOLDERK872990MICRINS SURGICAL SCISSOR

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

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

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