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FDA 510(k)

UNIGRIP-FH SURGICAL HANDPIECE/LAPAROSCOPIC

K-Number: K932604 · 1993-08-10

ApplicantUnisurge, Inc.
Decision Date1993-08-10
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

UNIGRIP-FH SURGICAL HANDPIECE/LAPAROSCOPIC is the device name listed in this FDA 510(k) record. The listed applicant is Unisurge, Inc.. It received FDA 510(k) clearance on 1993-08-10 under 510(k) number K932604. 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 UNIGRIP-FH SURGICAL HANDPIECE/LAPAROSCOPIC?

UNIGRIP-FH SURGICAL HANDPIECE/LAPAROSCOPIC is a medical device that received FDA 510(k) clearance on 1993-08-10. The listed applicant is Unisurge, Inc.. The 510(k) number is K932604.

When did UNIGRIP-FH SURGICAL HANDPIECE/LAPAROSCOPIC receive FDA 510(k) clearance?

UNIGRIP-FH SURGICAL HANDPIECE/LAPAROSCOPIC received FDA 510(k) clearance on 1993-08-10, under 510(k) number K932604.

Who is the listed applicant for UNIGRIP-FH SURGICAL HANDPIECE/LAPAROSCOPIC?

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

What is the FDA product code for UNIGRIP-FH SURGICAL HANDPIECE/LAPAROSCOPIC?

The FDA product code for UNIGRIP-FH SURGICAL HANDPIECE/LAPAROSCOPIC is GCJ.

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Other records listing Unisurge, Inc. as applicant

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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

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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