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FDA 510(k)

ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER GL4018

K-Number: K971212 · 1997-05-27

Decision Date1997-05-27
Product CodeMRZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER GL4018 is the device name listed in this FDA 510(k) record. The listed applicant is Alexander Mfg. Co.. It received FDA 510(k) clearance on 1997-05-27 under 510(k) number K971212. The device is classified under product code MRZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER GL4018?

ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER GL4018 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 K971212.

When did ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER GL4018 receive FDA 510(k) clearance?

ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER GL4018 received FDA 510(k) clearance on 1997-05-27, under 510(k) number K971212.

Who is the listed applicant for ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER GL4018?

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 PART NUMBER GL4018?

The FDA product code for ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER GL4018 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.

View all 39 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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