FDA 510(k)

TECHNA-CUT ASPIRATION NEEDLE

K-Number: K943651 · 1994-09-29

Decision Date1994-09-29

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

TECHNA-CUT ASPIRATION NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Manan Medical Products, Inc.. It received FDA 510(k) clearance on 1994-09-29 under 510(k) number K943651. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNA-CUT ASPIRATION NEEDLE?

TECHNA-CUT ASPIRATION NEEDLE is a medical device that received FDA 510(k) clearance on 1994-09-29. The listed applicant is Manan Medical Products, Inc.. The 510(k) number is K943651.

When did TECHNA-CUT ASPIRATION NEEDLE receive FDA 510(k) clearance?

TECHNA-CUT ASPIRATION NEEDLE received FDA 510(k) clearance on 1994-09-29, under 510(k) number K943651.

Who is the listed applicant for TECHNA-CUT ASPIRATION NEEDLE?

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

What is the FDA product code for TECHNA-CUT ASPIRATION NEEDLE?

The FDA product code for TECHNA-CUT ASPIRATION NEEDLE is KNW.

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Other records listing Manan Medical Products, Inc. as applicant

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Related Devices (Code: KNW)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.