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FDA 510(k)

SINGLE HAIR TRANSPLANT GRAFT

K-Number: K841741 · 1984-07-23

Decision Date1984-07-23
Product CodeFZT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SINGLE HAIR TRANSPLANT GRAFT is the device name listed in this FDA 510(k) record. The listed applicant is Paris Products, Inc.. It received FDA 510(k) clearance on 1984-07-23 under 510(k) number K841741. The device is classified under product code FZT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SINGLE HAIR TRANSPLANT GRAFT?

SINGLE HAIR TRANSPLANT GRAFT is a medical device that received FDA 510(k) clearance on 1984-07-23. The listed applicant is Paris Products, Inc.. The 510(k) number is K841741.

When did SINGLE HAIR TRANSPLANT GRAFT receive FDA 510(k) clearance?

SINGLE HAIR TRANSPLANT GRAFT received FDA 510(k) clearance on 1984-07-23, under 510(k) number K841741.

Who is the listed applicant for SINGLE HAIR TRANSPLANT GRAFT?

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

What is the FDA product code for SINGLE HAIR TRANSPLANT GRAFT?

The FDA product code for SINGLE HAIR TRANSPLANT GRAFT is FZT.

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: FZT)

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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