FDA 510(k)

STEREOMED CAMERA

K-Number: K823534 · 1982-12-15

ApplicantDiseases of the Skin Clinic, P.A.

Decision Date1982-12-15

Product CodeFTT

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

STEREOMED CAMERA is the device name listed in this FDA 510(k) record. The listed applicant is Diseases of the Skin Clinic, P.A.. It received FDA 510(k) clearance on 1982-12-15 under 510(k) number K823534. The device is classified under product code FTT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STEREOMED CAMERA?

STEREOMED CAMERA is a medical device that received FDA 510(k) clearance on 1982-12-15. The listed applicant is Diseases of the Skin Clinic, P.A.. The 510(k) number is K823534.

When did STEREOMED CAMERA receive FDA 510(k) clearance?

STEREOMED CAMERA received FDA 510(k) clearance on 1982-12-15, under 510(k) number K823534.

Who is the listed applicant for STEREOMED CAMERA?

The FDA 510(k) record lists Diseases of the Skin Clinic, P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STEREOMED CAMERA?

The FDA product code for STEREOMED CAMERA is FTT.

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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.