510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K770685Substantially Equivalent

Light, Examining, Dental, Ultra Violet

Parker Laboratories, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K770685 is the FDA 510(k) clearance record for LIGHT, EXAMINING, DENTAL, ULTRA VIOLET, a class II device, cleared for Parker Laboratories, Inc. on under FDA product code EAQ (Detector, Ultraviolet). FDA records list 30 510(k) clearances for Parker Laboratories, Inc., from to . As of , FDA records show no recalls naming K770685.

Clearance record

Decision date
Received
(14 days to decision)
Product code
EAQ Detector, Ultraviolet
Regulation
21 CFR 872.6350
Device class
Class II
Review panel
Dental
Applicant
Parker Laboratories, Inc. 803 N. Front St. Suite 3, Mchenry IL
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