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FDA 510(k)

GYRUS OPEN FORCEPS

K-Number: K024286 · 2003-11-17

ApplicantGyrus Medical, Inc.
Decision Date2003-11-17
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GYRUS OPEN FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Gyrus Medical, Inc.. It received FDA 510(k) clearance on 2003-11-17 under 510(k) number K024286. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GYRUS OPEN FORCEPS?

GYRUS OPEN FORCEPS is a medical device that received FDA 510(k) clearance on 2003-11-17. The listed applicant is Gyrus Medical, Inc.. The 510(k) number is K024286.

When did GYRUS OPEN FORCEPS receive FDA 510(k) clearance?

GYRUS OPEN FORCEPS received FDA 510(k) clearance on 2003-11-17, under 510(k) number K024286.

Who is the listed applicant for GYRUS OPEN FORCEPS?

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

What is the FDA product code for GYRUS OPEN FORCEPS?

The FDA product code for GYRUS OPEN FORCEPS is GEI.

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Other records listing Gyrus Medical, 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.

K050550GYRUS GENERAL PURPOSE ELECTROSURGICAL GENERATORK050460GYRUS PLASMACISION AND PLASMABLEND ELECTRODESK041999GYRUS PLASMA SKIN RESURFACING SYSTEMK041633GYRUS PLASMACISION LAPAROSCOPIC SPATULAK031085GYRUS PLASMAKINETIC SUPERPULSE SYSTEM (GENERATOR, ACCESSORIES)K031082EVEREST BIPOLAR L HOOK & PK BIPOLAR L HOOK

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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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