510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K852534Substantially Equivalent

Ultraviolet Treatment Lamps UV-8 & UV-9

R. A. Fischer Co. Corp., Glendale CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K852534 is the FDA 510(k) clearance record for ULTRAVIOLET TREATMENT LAMPS UV-8 & UV-9, a class II device, cleared for R. A. Fischer Co. Corp. on under FDA product code FTC (Light, Ultraviolet, Dermatological). FDA records list 13 510(k) clearances for R. A. Fischer Co. Corp., from to . As of , FDA records show no recalls naming K852534.

Clearance record

Decision date
Received
(147 days to decision)
Product code
FTC Light, Ultraviolet, Dermatological
Regulation
21 CFR 878.4630
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
R. A. Fischer Co. Corp. 517 Commercial St., Glendale CA
Third party review
No

Clearances, product code FTC

Trailing 12 months
2 clearances under product code FTC in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FTC, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260