510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K881467Substantially Equivalent

Microscope Stage Heater

Cryodyne Technologies, Inc., Soquel CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K881467 is the FDA 510(k) clearance record for MICROSCOPE STAGE HEATER, a class I device, cleared for Cryodyne Technologies, Inc. on under FDA product code KEJ (Stages, Microscope). FDA records list 6 510(k) clearances for Cryodyne Technologies, Inc., from to . As of , FDA records show no recalls naming K881467.

Clearance record

Decision date
Received
(12 days to decision)
Product code
KEJ Stages, Microscope
Regulation
21 CFR 864.3600
Device class
Class I
Review panel
Pathology
Applicant
Cryodyne Technologies, Inc. 400 Hoover Rd., Soquel CA
Third party review
No

Clearances, product code KEJ

Trailing 12 months

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

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