510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K790103Substantially Equivalent

Nephelometer, Mic-2000 Laser

Dynatech Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K790103 is the FDA 510(k) clearance record for NEPHELOMETER, MIC-2000 LASER, a class I device, cleared for Dynatech Corp. on under FDA product code JQX (Nephelometer, For Clinical Use). FDA records list 27 510(k) clearances for Dynatech Corp., from to . As of , FDA records show no recalls naming K790103.

Clearance record

Decision date
Received
(55 days to decision)
Product code
JQX Nephelometer, For Clinical Use
Regulation
21 CFR 862.2700
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Dynatech Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JQX

Trailing 12 months

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

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