510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K934728Substantially Equivalent

Sunsor Ultraviolet Meter

Sunsor, Inc., Pittsburgh PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K934728 is the FDA 510(k) clearance record for SUNSOR ULTRAVIOLET METER, a class II device, cleared for Sunsor, Inc. on under FDA product code EAQ (Detector, Ultraviolet). FDA records list one 510(k) clearance for Sunsor, Inc. As of , FDA records show no recalls naming K934728.

Clearance record

Decision date
Received
(302 days to decision)
Product code
EAQ Detector, Ultraviolet
Regulation
21 CFR 872.6350
Device class
Class II
Review panel
Dental
Applicant
Sunsor, Inc. 1388 Freeport Rd., Pittsburgh PA
510(k) summary
Summary
Third party review
No

Clearances, product code EAQ

Trailing 12 months

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

FDA records show no clearances under product code EAQ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EAQ, 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