ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY # GL825-P
K-Number: K971213 · 1997-05-27
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Device Summary
Frequently Asked Questions
What is the ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY # GL825-P?
ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY # GL825-P is a medical device that received FDA 510(k) clearance on 1997-05-27. The listed applicant is Alexander Mfg. Co.. The 510(k) number is K971213.
When did ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY # GL825-P receive FDA 510(k) clearance?
ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY # GL825-P received FDA 510(k) clearance on 1997-05-27, under 510(k) number K971213.
Who is the listed applicant for ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY # GL825-P?
The FDA 510(k) record lists Alexander Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY # GL825-P?
The FDA product code for ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY # GL825-P is MRZ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Alexander Mfg. Co. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: MRZ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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