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FDA 510(k)

R&D BATTERIES, INC. PART NUMBERS 5213, 5222, 5268 AND 5284

K-Number: K951278 · 1995-08-18

Decision Date1995-08-18
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

R&D BATTERIES, INC. PART NUMBERS 5213, 5222, 5268 AND 5284 is the device name listed in this FDA 510(k) record. The listed applicant is R & D Batteries, Inc.. It received FDA 510(k) clearance on 1995-08-18 under 510(k) number K951278. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the R&D BATTERIES, INC. PART NUMBERS 5213, 5222, 5268 AND 5284?

R&D BATTERIES, INC. PART NUMBERS 5213, 5222, 5268 AND 5284 is a medical device that received FDA 510(k) clearance on 1995-08-18. The listed applicant is R & D Batteries, Inc.. The 510(k) number is K951278.

When did R&D BATTERIES, INC. PART NUMBERS 5213, 5222, 5268 AND 5284 receive FDA 510(k) clearance?

R&D BATTERIES, INC. PART NUMBERS 5213, 5222, 5268 AND 5284 received FDA 510(k) clearance on 1995-08-18, under 510(k) number K951278.

Who is the listed applicant for R&D BATTERIES, INC. PART NUMBERS 5213, 5222, 5268 AND 5284?

The FDA 510(k) record lists R & D Batteries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for R&D BATTERIES, INC. PART NUMBERS 5213, 5222, 5268 AND 5284?

The FDA product code for R&D BATTERIES, INC. PART NUMBERS 5213, 5222, 5268 AND 5284 is FLL.

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 R & D Batteries, 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.

View all 52 devices →

Related Devices (Code: FLL)

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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