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FDA 510(k)

BATTERY, RECHARGEABLE

K-Number: K030261 · 2003-04-24

ApplicantAccess Battery, Inc.
Decision Date2003-04-24
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

BATTERY, RECHARGEABLE is the device name listed in this FDA 510(k) record. The listed applicant is Access Battery, Inc.. It received FDA 510(k) clearance on 2003-04-24 under 510(k) number K030261. The device is classified under product code HGM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BATTERY, RECHARGEABLE?

BATTERY, RECHARGEABLE is a medical device that received FDA 510(k) clearance on 2003-04-24. The listed applicant is Access Battery, Inc.. The 510(k) number is K030261.

When did BATTERY, RECHARGEABLE receive FDA 510(k) clearance?

BATTERY, RECHARGEABLE received FDA 510(k) clearance on 2003-04-24, under 510(k) number K030261.

Who is the listed applicant for BATTERY, RECHARGEABLE?

The FDA 510(k) record lists Access Battery, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BATTERY, RECHARGEABLE?

The FDA product code for BATTERY, RECHARGEABLE is HGM.

Related Clinical Trials

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Other records listing Access Battery, Inc. 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.

K032051BATTERY PACK, RECHARGEABLE, MODELS MLA0051, MLA90479, MNC5169L/P, MNC1000EKG, MNC14649P

Related Devices (Code: HGM)

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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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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