510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K760908Substantially Equivalent

Miniature Ascending Paper Chromato-

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

K760908 is the FDA 510(k) clearance record for MINIATURE ASCENDING PAPER CHROMATO-, a class I device, cleared for Ackerman Nuclear, Inc. on under FDA product code DPA (Apparatus, General Use, Thin Layer Chromatography). FDA records list one 510(k) clearance for Ackerman Nuclear, Inc. As of , FDA records show no recalls naming K760908.

Clearance record

Decision date
Received
(24 days to decision)
Product code
DPA Apparatus, General Use, Thin Layer Chromatography
Regulation
21 CFR 862.2270
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Ackerman Nuclear, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DPA

Trailing 12 months

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

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