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FDA 510(k)

CALVITRON HAIR TRANSPLANT SYSTEM

K-Number: K952737 · 1995-10-03

Decision Date1995-10-03
Product CodeGAH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CALVITRON HAIR TRANSPLANT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medicamat S.A.. It received FDA 510(k) clearance on 1995-10-03 under 510(k) number K952737. 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 CALVITRON HAIR TRANSPLANT SYSTEM?

CALVITRON HAIR TRANSPLANT SYSTEM is a medical device that received FDA 510(k) clearance on 1995-10-03. The listed applicant is Medicamat S.A.. The 510(k) number is K952737.

When did CALVITRON HAIR TRANSPLANT SYSTEM receive FDA 510(k) clearance?

CALVITRON HAIR TRANSPLANT SYSTEM received FDA 510(k) clearance on 1995-10-03, under 510(k) number K952737.

Who is the listed applicant for CALVITRON HAIR TRANSPLANT SYSTEM?

The FDA 510(k) record lists Medicamat S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CALVITRON HAIR TRANSPLANT SYSTEM?

The FDA product code for CALVITRON HAIR TRANSPLANT SYSTEM 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.

Other records listing Medicamat S.A. as applicant

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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