510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K823534Substantially Equivalent

Stereomed Camera

Diseases of the Skin Clinic, P.A., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K823534 is the FDA 510(k) clearance record for STEREOMED CAMERA, a class I device, cleared for Diseases of the Skin Clinic, P.A. on under FDA product code FTT (Camera, Still, Surgical). FDA records list one 510(k) clearance for Diseases of the Skin Clinic, P.A. As of , FDA records show no recalls naming K823534.

Clearance record

Decision date
Received
(25 days to decision)
Product code
FTT Camera, Still, Surgical
Regulation
21 CFR 878.4160
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Diseases of the Skin Clinic, P.A. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code FTT

Trailing 12 months

FDA records hold no clearances under product code FTT in the trailing twelve months.

FDA records show no clearances under product code FTT in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FTT, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260