510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K935427Substantially Equivalent

R and D Batteries

R & D Batteries, Inc., Burnsville MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K935427 is the FDA 510(k) clearance record for R AND D BATTERIES, a class II device, cleared for R & D Batteries, Inc. on under FDA product code JAF (Monitor, Ultrasonic, Nonfetal). FDA records list 53 510(k) clearances for R & D Batteries, Inc., from to . As of , FDA records show no recalls naming K935427.

Clearance record

Decision date
Received
(345 days to decision)
Product code
JAF Monitor, Ultrasonic, Nonfetal
Regulation
21 CFR 892.1540
Device class
Class II
Review panel
Radiology
Applicant
R & D Batteries, Inc. P.O. Box 5007, Burnsville MN
510(k) summary
Statement
Third party review
No

Clearances, product code JAF

Trailing 12 months

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

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