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FDA 510(k)

R&D PART NOS. 5339, 5510, 5514

K-Number: K945871 · 1995-02-27

ApplicantR & D Batteries, Inc.
Decision Date1995-02-27
Product CodeFCO
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

R&D PART NOS. 5339, 5510, 5514 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 1995-02-27 under 510(k) number K945871. The device is classified under product code FCO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the R&D PART NOS. 5339, 5510, 5514?

R&D PART NOS. 5339, 5510, 5514 is a medical device that received FDA 510(k) clearance on 1995-02-27. The listed applicant is R & D Batteries, Inc.. The 510(k) number is K945871.

When did R&D PART NOS. 5339, 5510, 5514 receive FDA 510(k) clearance?

R&D PART NOS. 5339, 5510, 5514 received FDA 510(k) clearance on 1995-02-27, under 510(k) number K945871.

Who is the listed applicant for R&D PART NOS. 5339, 5510, 5514?

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 PART NOS. 5339, 5510, 5514?

The FDA product code for R&D PART NOS. 5339, 5510, 5514 is FCO.

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.

K951284R&D BATTERIES, INC. PART NUMBERS 5137, 5140, 5142 AND 5155K951277R&D BATTERIES, INC. PART NUMBERS 5295, 5334, 5344 AND 5410K951278R&D BATTERIES, INC. PART NUMBERS 5213, 5222, 5268 AND 5284K951280R&D BATTERIES, INC. PART NUMBERS 5003, 5006, 5008 AND 5012K951285R&D BATTERIES, INC. PART NUMBERS 5158, 5168, 5171 AND 5172K951276R&D BATTERIES, INC. PART NUMBERS 5412, 5420, 5436 AND 5438

View all 52 devices →

Related Devices (Code: FCO)

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.

K946080PHYSIO CONTROL LIFEPAK 200 AUTO DEFIBRILLATORPortable Power Systems, Inc.K945870R&D PART NOS. 5490, 5541, 5358, 5497R & D Batteries, Inc.K944388R&D BATTERIES PART NOS. 5116, 5124, 5099, 5100R & D Batteries, Inc.K944348R&D BATTERIES, INC. PART NO. 5128, 5053, 5007R & D Batteries, Inc.K944389R&D BATTERIES PART NOS. 5111, 5112, 5065, 5153R & D Batteries, Inc.K945868R&D PART NOS. 5262, 5543, 5432, 5469R & D Batteries, 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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