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FDA 510(k)

R AND D BATTERIES

K-Number: K935427 · 1994-10-21

ApplicantR & D Batteries, Inc.
Decision Date1994-10-21
Product CodeJAF
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

R AND D BATTERIES 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 1994-10-21 under 510(k) number K935427. The device is classified under product code JAF. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the R AND D BATTERIES?

R AND D BATTERIES is a medical device that received FDA 510(k) clearance on 1994-10-21. The listed applicant is R & D Batteries, Inc.. The 510(k) number is K935427.

When did R AND D BATTERIES receive FDA 510(k) clearance?

R AND D BATTERIES received FDA 510(k) clearance on 1994-10-21, under 510(k) number K935427.

Who is the listed applicant for R AND D BATTERIES?

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 AND D BATTERIES?

The FDA product code for R AND D BATTERIES is JAF.

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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: JAF)

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.

K242487Laminar P1 (LDH-HW-001)Laminar Digital Health, Inc.K110628SIMPLEABINewman MedicalK093393LIFEDOP MODEL 300ABISummit Doppler Systems, Inc.K090009THD SLIDE ONEThd SpaK081429THD SLIDEThd SpaK070815THDG.F. S.R.L.

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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