510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K893874Substantially Equivalent

Fujitens III

Altoona Medical Supply, Altoona IA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K893874 is the FDA 510(k) clearance record for FUJITENS III, a class II device, cleared for Altoona Medical Supply on under FDA product code GZQ (Instrument, Dowel Cutting). FDA records list 3 510(k) clearances for Altoona Medical Supply, from to . As of , FDA records show no recalls naming K893874.

Clearance record

Decision date
Received
(210 days to decision)
Product code
GZQ Instrument, Dowel Cutting
Regulation
21 CFR 882.4275
Device class
Class II
Review panel
Neurology
Applicant
Altoona Medical Supply 705 2nd Ave., SW, Altoona IA
Third party review
No

Clearances, product code GZQ

Trailing 12 months

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

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