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FDA 510(k)

ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY #M12/630

K-Number: K973851 · 1998-01-05

ApplicantAlexander Mfg. Co.
Decision Date1998-01-05
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY #M12/630 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 1998-01-05 under 510(k) number K973851. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY #M12/630?

ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY #M12/630 is a medical device that received FDA 510(k) clearance on 1998-01-05. The listed applicant is Alexander Mfg. Co.. The 510(k) number is K973851.

When did ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY #M12/630 receive FDA 510(k) clearance?

ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY #M12/630 received FDA 510(k) clearance on 1998-01-05, under 510(k) number K973851.

Who is the listed applicant for ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY #M12/630?

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 #M12/630?

The FDA product code for ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY #M12/630 is FRN.

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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 GL825-200K973850ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY #M007

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Related Devices (Code: FRN)

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.

K253703RemunityPRO+ Pump for Remodulin® (treprostinil) InjectionDeka R&D CorpK252015FreedomEdge Infusion System; High-Flo SubQ Needle Set; Precision Flow Rate TubingKoru Medical Systems, Inc.K251636Spectrum IQ Infusion System with Dose IQ Safety Software (3570009)Baxter Healthcare CorporationK251640SIGMA Spectrum Infusion Pump with Master Drug LibraryBaxter Healthcare CorporationK242752MRidium 3870 MRI Infusion Pump System (3870)Iradimed CorporationK243855BD Alaris Infusion System with Guardrails Suite MXCarefusion 303, 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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