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FDA 510(k)

RAPID FIRE HAIR IMPLANTER CAROUSEL

K-Number: K972918 · 1997-10-27

Decision Date1997-10-27
Product CodeGAH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RAPID FIRE HAIR IMPLANTER CAROUSEL is the device name listed in this FDA 510(k) record. The listed applicant is Apex Medical Products, LLC. It received FDA 510(k) clearance on 1997-10-27 under 510(k) number K972918. The device is classified under product code GAH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAPID FIRE HAIR IMPLANTER CAROUSEL?

RAPID FIRE HAIR IMPLANTER CAROUSEL is a medical device that received FDA 510(k) clearance on 1997-10-27. The listed applicant is Apex Medical Products, LLC. The 510(k) number is K972918.

When did RAPID FIRE HAIR IMPLANTER CAROUSEL receive FDA 510(k) clearance?

RAPID FIRE HAIR IMPLANTER CAROUSEL received FDA 510(k) clearance on 1997-10-27, under 510(k) number K972918.

Who is the listed applicant for RAPID FIRE HAIR IMPLANTER CAROUSEL?

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

What is the FDA product code for RAPID FIRE HAIR IMPLANTER CAROUSEL?

The FDA product code for RAPID FIRE HAIR IMPLANTER CAROUSEL is GAH.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: GAH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

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