Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K980224Substantially Equivalent

Alexander Manufacturing Co. Rechargeable Battery Part Number Ms822

Alexander Mfg. Co., Mason City IA / Traditional, Substantially Equivalent

K980224 is the FDA 510(k) clearance record for ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS822, a class I device, cleared for Alexander Mfg. Co. on under FDA product code MOQ (Battery, Replacement, Rechargeable). FDA records list 39 510(k) clearances for Alexander Mfg. Co., from to . As of , FDA records show no recalls naming K980224.

Clearance record

Decision date
Received
(70 days to decision)
Product code
MOQ Battery, Replacement, Rechargeable
Regulation
21 CFR 878.4820
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Alexander Mfg. Co. 1511 S Garfield Pl., Mason City IA
510(k) summary
Statement
Third party review
No

Clearances, product code MOQ

Trailing 12 months

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

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