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FDA 510(k)

DETACHATIP THORACOSCOPIC SCISSORS

K-Number: K960554 · 1996-03-05

ApplicantMicrosurge, Inc.
Decision Date1996-03-05
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DETACHATIP THORACOSCOPIC SCISSORS is the device name listed in this FDA 510(k) record. The listed applicant is Microsurge, Inc.. It received FDA 510(k) clearance on 1996-03-05 under 510(k) number K960554. 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 DETACHATIP THORACOSCOPIC SCISSORS?

DETACHATIP THORACOSCOPIC SCISSORS is a medical device that received FDA 510(k) clearance on 1996-03-05. The listed applicant is Microsurge, Inc.. The 510(k) number is K960554.

When did DETACHATIP THORACOSCOPIC SCISSORS receive FDA 510(k) clearance?

DETACHATIP THORACOSCOPIC SCISSORS received FDA 510(k) clearance on 1996-03-05, under 510(k) number K960554.

Who is the listed applicant for DETACHATIP THORACOSCOPIC SCISSORS?

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 DETACHATIP THORACOSCOPIC SCISSORS?

The FDA product code for DETACHATIP THORACOSCOPIC SCISSORS is GEI.

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Other records listing Microsurge, Inc. as applicant

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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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