510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K951194Substantially Equivalent

Fi-10M

Pentax Precision Instrument Corp., Miramar FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K951194 is the FDA 510(k) clearance record for FI-10M, a class I device, cleared for Pentax Precision Instrument Corp. on under FDA product code CAL (Laryngoscope, Non-Rigid). FDA records list 67 510(k) clearances for Pentax Precision Instrument Corp., from to . As of , FDA records show no recalls naming K951194.

Clearance record

Decision date
Received
(21 days to decision)
Product code
CAL Laryngoscope, Non-Rigid
Regulation
21 CFR 868.5530
Device class
Class I
Review panel
Anesthesiology
Applicant
Pentax Precision Instrument Corp. 3117 Commerce Pkwy., Miramar FL
510(k) summary
Summary
Third party review
No

Clearances, product code CAL

Trailing 12 months

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

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