510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K971240Substantially Equivalent

Alexander Manufacturing Co. Rechargeable Battery Part Number M006

Alexander Mfg. Co., Mason City IA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K971240 is the FDA 510(k) clearance record for ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M006, a class II device, cleared for Alexander Mfg. Co. on under FDA product code HEL (Monitor, Heart Rate, Fetal, Ultrasonic). FDA records list 39 510(k) clearances for Alexander Mfg. Co., from to . As of , FDA records show no recalls naming K971240.

Clearance record

Decision date
Received
(65 days to decision)
Product code
HEL Monitor, Heart Rate, Fetal, Ultrasonic
Regulation
21 CFR 884.2660
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Alexander Mfg. Co. 1511 S Garfield Pl., Mason City IA
510(k) summary
Statement
Third party review
No

Clearances, product code HEL

Trailing 12 months

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

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