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FDA 510(k)

ALEXANDER MFG. RECHARGEABLE BATTERY (MODEL M3)

K-Number: K970787 · 1997-05-14

ApplicantAlexander Mfg. Co.
Decision Date1997-05-14
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ALEXANDER MFG. RECHARGEABLE BATTERY (MODEL M3) 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 1997-05-14 under 510(k) number K970787. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALEXANDER MFG. RECHARGEABLE BATTERY (MODEL M3)?

ALEXANDER MFG. RECHARGEABLE BATTERY (MODEL M3) is a medical device that received FDA 510(k) clearance on 1997-05-14. The listed applicant is Alexander Mfg. Co.. The 510(k) number is K970787.

When did ALEXANDER MFG. RECHARGEABLE BATTERY (MODEL M3) receive FDA 510(k) clearance?

ALEXANDER MFG. RECHARGEABLE BATTERY (MODEL M3) received FDA 510(k) clearance on 1997-05-14, under 510(k) number K970787.

Who is the listed applicant for ALEXANDER MFG. RECHARGEABLE BATTERY (MODEL M3)?

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 MFG. RECHARGEABLE BATTERY (MODEL M3)?

The FDA product code for ALEXANDER MFG. RECHARGEABLE BATTERY (MODEL M3) is DPS.

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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: DPS)

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.

K254255S-Patch CardioAIWellysis Corp.K252463SE-1202 Series Electrocardiograph (Model: SE-1202, SE-1202E)Edan Instruments, Inc.K251670MAC 7 Resting ECG Analysis SystemGe Medical Systems Information Technologies, Inc.K252361AccurECG Analysis System (v2.0)Accurkardia, Inc.K252474Withings BeamO (SCT02)WithingsK250569Cardiologs Holter PlatformPhilips France Commercial

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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