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FDA 510(k)

MICROSURGE BIPOLAR GRASPERS

K-Number: K951230 · 1995-06-14

ApplicantMicrosurge, Inc.
Decision Date1995-06-14
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICROSURGE BIPOLAR GRASPERS is the device name listed in this FDA 510(k) record. The listed applicant is Microsurge, Inc.. It received FDA 510(k) clearance on 1995-06-14 under 510(k) number K951230. 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 MICROSURGE BIPOLAR GRASPERS?

MICROSURGE BIPOLAR GRASPERS is a medical device that received FDA 510(k) clearance on 1995-06-14. The listed applicant is Microsurge, Inc.. The 510(k) number is K951230.

When did MICROSURGE BIPOLAR GRASPERS receive FDA 510(k) clearance?

MICROSURGE BIPOLAR GRASPERS received FDA 510(k) clearance on 1995-06-14, under 510(k) number K951230.

Who is the listed applicant for MICROSURGE BIPOLAR GRASPERS?

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

What is the FDA product code for MICROSURGE BIPOLAR GRASPERS?

The FDA product code for MICROSURGE BIPOLAR GRASPERS is GEI.

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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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