Alexander Manufacturing Co. Rechargeable Battery Part Number STR5

FDA 510(k) K971107 · Alexander Mfg. Co.

Substantially Equivalent

510(k) numberK971107

Submission

Device name
Alexander Manufacturing Co. Rechargeable Battery Part Number STR5
Applicant
Alexander Mfg. Co.
Mason City, IA, US
Received
March 26, 1997
Decision date
June 5, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
BTA – Pump, Portable, Aspiration (Manual Or Powered)
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4780
Specialty
General, Plastic Surgery

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More from Shenzhen Kingboom Technology Co., Ltd.

510(k)DeviceDecision
K982896Alexander Manufacturing Co. Rechargeable Battery Part Number LP9LDD · Traditional 10/21/1998ST
K981776Alexander Manufacturing Co. Battery Part Number MC146XFRN · Traditional 08/03/1998SE
K981728Alexander Manufacturing Co. Battery Part Number H134BZQ · Traditional 06/26/1998ST
K980224Alexander Manufacturing Co. Rechargeable Battery Part Number MS822MOQ · Traditional 04/02/1998SE
K974061Rechargeable Battery Part Number GL825-200DXN · Traditional 01/16/1998SE
K973851Alexander Manufacturing Co. Rechargeable Battery #M12/630FRN · Traditional 01/05/1998SE
K973850Alexander Manufacturing Co. Rechargeable Battery #M007HFO · Traditional 11/12/1997SE
K972746Alexander Manufacturing Co. Rechargeable Battery Part Number LP6/100DPS · Traditional 10/21/1997SE
K972780Alexander Manufacturing Co. Rechargeable Battery Part Number GL625MRZ · Traditional 10/20/1997SE
K972779Alexander Manufacturing Co. Rechargeable Battery Part Number MS3030-PMRZ · Traditional 10/20/1997SE

Questions and answers

When was Alexander Manufacturing Co. Rechargeable Battery Part Number STR5 cleared by the FDA?

Alexander Manufacturing Co. Rechargeable Battery Part Number STR5 (K971107) received a 510(k) decision of Substantially Equivalent on June 5, 1997, 71 days after the submission was received.

What is the product code of K971107?

The FDA product code is BTA – Pump, Portable, Aspiration (Manual Or Powered), a Class II (moderate risk) device regulated under 21 CFR 878.4780.