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FDA 510(k)

HOLMED HAND HELD INSTRUMENTS

K-Number: K913810 · 1991-12-19

ApplicantPerformance Surgical Instruments Corp.
Decision Date1991-12-19
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HOLMED HAND HELD INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Performance Surgical Instruments Corp.. It received FDA 510(k) clearance on 1991-12-19 under 510(k) number K913810. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOLMED HAND HELD INSTRUMENTS?

HOLMED HAND HELD INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1991-12-19. The listed applicant is Performance Surgical Instruments Corp.. The 510(k) number is K913810.

When did HOLMED HAND HELD INSTRUMENTS receive FDA 510(k) clearance?

HOLMED HAND HELD INSTRUMENTS received FDA 510(k) clearance on 1991-12-19, under 510(k) number K913810.

Who is the listed applicant for HOLMED HAND HELD INSTRUMENTS?

The FDA 510(k) record lists Performance Surgical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HOLMED HAND HELD INSTRUMENTS?

The FDA product code for HOLMED HAND HELD INSTRUMENTS is GCJ.

Related Clinical Trials

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Other records listing Performance Surgical Instruments Corp. 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.

K934737LASSO (SCHWAITZBERG) SUTURE SNARE

Related Devices (Code: GCJ)

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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Official Source

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