ALEXANDER BOX, BATTERY, RECHARGEABLE— 510(k) K963305

Name: FDA 510(k) clearance K963305
Creator: U.S. Food and Drug Administration
Published: 1997-04-17

Substantially Equivalent

Alexander Mfg. Co.

FDA 510(k) clearance K963305 for ALEXANDER BOX, BATTERY, RECHARGEABLE, Substantially Equivalent on 1997-04-17. Applicant: Alexander Mfg. Co.. Device class: 2.

Clearance details

Applicant: Alexander Mfg. Co.
Product code: Code BWA
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 1996-08-22
Decision date: 1997-04-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mason City, IA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BWA

view all

K874794 — E600B FOOTSWITCH1987-12-14
K873809 — EXCALIBUR ELECTROSURGICAL UNIT 60-5200-0011987-11-20

More clearances from Alexander Mfg. Co.

view all

K982896 — ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER LP91998-10-21
K981776 — ALEXANDER MANUFACTURING CO. BATTERY PART NUMBER MC146X1998-08-03
K981728 — ALEXANDER MANUFACTURING CO. BATTERY PART NUMBER H1341998-06-26
K980224 — ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS8221998-04-02
K974061 — RECHARGEABLE BATTERY PART NUMBER GL825-2001998-01-16

Data sourced from openFDA. This site is unofficial and independent of the FDA.