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Alexander Manufacturing Co. Rechargeable Battery Part Number MS3030-P

by Alexander Mfg. Co.

510(k) K972779

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK972779 Date20 Oct 1997ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
MRZ
Device Class
Class II
Regulation
21 CFR Part 880.5725
Advisory Committee
General Hospital
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 26 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The Alexander Manufacturing Co. Rechargeable Battery Part Number MS3030-P is a replacement power source designed for use with Corpak 415A R200 and VTR300D enteral pumps. This device provides electrical power to maintain pump function in clinical settings.

The device is operated by biomedical equipment technicians and is classified as a class II medical device with FDA 510(k) clearance. It is regulated under product code MRZ and regulation number 880.5725, with a decision of substantial equivalence made on October 20, 1997.

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