510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K100563Substantially Equivalent

Geon Rapid Digital Thermometer Model: Mt-B117, Mt-B127, Mt-B130, Mt-B132fa

Geon Corporation, Flagstaff AZ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K100563 is the FDA 510(k) clearance record for GEON RAPID DIGITAL THERMOMETER MODEL: MT-B117, MT-B127, MT-B130, MT-B132FA, a class II device, cleared for Geon Corporation on under FDA product code FLL (Continuous Measurement Thermometer). FDA's definition for product code FLL reads: "A continuous measurement thermometer is a clinical electronic thermometer indicated to measure the body or skin temperature of a person continuously or in specified intervals. Under this regulation, this product code represents non-exempt...". FDA records list one 510(k) clearance for Geon Corporation. As of , FDA records show no recalls naming K100563.

Clearance record

Decision date
Received
(93 days to decision)
Product code
FLL Continuous Measurement Thermometer
Regulation
21 CFR 880.2910
Device class
Class II
Review panel
General Hospital
Applicant
Geon Corporation 2904 N. Boldt Dr., Flagstaff AZ
510(k) summary
Statement
Third party review
No

Clearances, product code FLL

Trailing 12 months
2 clearances under product code FLL in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FLL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260