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FDA 510(k)

MICROSURGE VERESS NEEDLE

K-Number: K954520 · 1995-10-16

ApplicantMicrosurge, Inc.
Decision Date1995-10-16
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MICROSURGE VERESS NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Microsurge, Inc.. It received FDA 510(k) clearance on 1995-10-16 under 510(k) number K954520. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROSURGE VERESS NEEDLE?

MICROSURGE VERESS NEEDLE is a medical device that received FDA 510(k) clearance on 1995-10-16. The listed applicant is Microsurge, Inc.. The 510(k) number is K954520.

When did MICROSURGE VERESS NEEDLE receive FDA 510(k) clearance?

MICROSURGE VERESS NEEDLE received FDA 510(k) clearance on 1995-10-16, under 510(k) number K954520.

Who is the listed applicant for MICROSURGE VERESS NEEDLE?

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 VERESS NEEDLE?

The FDA product code for MICROSURGE VERESS NEEDLE is HET.

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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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