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FDA 510(k)

R AND D BATTERY REPLACEMENT

K-Number: K933337 · 1994-04-05

ApplicantR & D Batteries, Inc.
Decision Date1994-04-05
Product CodeKIJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

R AND D BATTERY REPLACEMENT 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 1994-04-05 under 510(k) number K933337. The device is classified under product code KIJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the R AND D BATTERY REPLACEMENT?

R AND D BATTERY REPLACEMENT is a medical device that received FDA 510(k) clearance on 1994-04-05. The listed applicant is R & D Batteries, Inc.. The 510(k) number is K933337.

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

R AND D BATTERY REPLACEMENT received FDA 510(k) clearance on 1994-04-05, under 510(k) number K933337.

Who is the listed applicant for R AND D BATTERY REPLACEMENT?

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 BATTERY REPLACEMENT?

The FDA product code for R AND D BATTERY REPLACEMENT is KIJ.

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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: KIJ)

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.

K163308SMARTOJeil Medical CorporationK112599INSURGICAL SINGLE USE POWER EQUIPMENTInsurgical, LLCK101563SMARTOJeil Medical CorporationK972367STRYKER SYSTEM 4000 HEAVY DUTY BATTERY POWERED EQUIPMENTStryker InstrumentsK970378STRYKER 2115 REPLACEMENT BATTERY (2115)Implant Resource, Inc.K960711ACUMED BONE GRAFT SYSTEMAcu Med, 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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