FDA 510(k)

NEEDLE, ACUPUNCTURE

K-Number: K964051 · 1996-11-05

Decision Date1996-11-05

Product CodeMQX

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

NEEDLE, ACUPUNCTURE is the device name listed in this FDA 510(k) record. The listed applicant is S-Tcm Enterprises, Inc.. It received FDA 510(k) clearance on 1996-11-05 under 510(k) number K964051. The device is classified under product code MQX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEEDLE, ACUPUNCTURE?

NEEDLE, ACUPUNCTURE is a medical device that received FDA 510(k) clearance on 1996-11-05. The listed applicant is S-Tcm Enterprises, Inc.. The 510(k) number is K964051.

When did NEEDLE, ACUPUNCTURE receive FDA 510(k) clearance?

NEEDLE, ACUPUNCTURE received FDA 510(k) clearance on 1996-11-05, under 510(k) number K964051.

Who is the listed applicant for NEEDLE, ACUPUNCTURE?

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

What is the FDA product code for NEEDLE, ACUPUNCTURE?

The FDA product code for NEEDLE, ACUPUNCTURE is MQX.

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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.