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FDA 510(k)

ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500-3P

K-Number: K971865 · 1997-07-03

ApplicantAlexander Mfg. Co.
Decision Date1997-07-03
Product CodeLDR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500-3P 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 1997-07-03 under 510(k) number K971865. The device is classified under product code LDR. 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 M12/500-3P?

ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500-3P is a medical device that received FDA 510(k) clearance on 1997-07-03. The listed applicant is Alexander Mfg. Co.. The 510(k) number is K971865.

When did ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500-3P receive FDA 510(k) clearance?

ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500-3P received FDA 510(k) clearance on 1997-07-03, under 510(k) number K971865.

Who is the listed applicant for ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500-3P?

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 M12/500-3P?

The FDA product code for ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500-3P is LDR.

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.

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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.

K982896ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER LP9K981776ALEXANDER MANUFACTURING CO. BATTERY PART NUMBER MC146XK981728ALEXANDER MANUFACTURING CO. BATTERY PART NUMBER H134K980224ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS822K974061RECHARGEABLE BATTERY PART NUMBER GL825-200K973851ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY #M12/630

View all 39 devices →

Related Devices (Code: LDR)

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.

K242693DEKA Infusion System, DEKA Administration SetDeka Research and Development CorporationK232316DEKA Infusion System, DEKA Administration SetDeka Research and DevelopmentK153760Volumetric Infusion ControllerDEKA Research & DevelopmentK963136PACER MODEL 100 INFUSION CONTROLLERHealth Watch, Inc.K971826ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500Alexander Mfg. Co.K934543UNIVERSAL CONTROLLER, MODEL 100Metamed, Inc.

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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