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FDA 510(k)

REPLACEMENT BATTERIES PART NO. 5098,5135, 5097

K-Number: K936018 · 1994-02-22

ApplicantR & D Batteries, Inc.
Decision Date1994-02-22
Product CodeHLJ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

REPLACEMENT BATTERIES PART NO. 5098,5135, 5097 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 1994-02-22 under 510(k) number K936018. The device is classified under product code HLJ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPLACEMENT BATTERIES PART NO. 5098,5135, 5097?

REPLACEMENT BATTERIES PART NO. 5098,5135, 5097 is a medical device that received FDA 510(k) clearance on 1994-02-22. The listed applicant is R & D Batteries, Inc.. The 510(k) number is K936018.

When did REPLACEMENT BATTERIES PART NO. 5098,5135, 5097 receive FDA 510(k) clearance?

REPLACEMENT BATTERIES PART NO. 5098,5135, 5097 received FDA 510(k) clearance on 1994-02-22, under 510(k) number K936018.

Who is the listed applicant for REPLACEMENT BATTERIES PART NO. 5098,5135, 5097?

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 REPLACEMENT BATTERIES PART NO. 5098,5135, 5097?

The FDA product code for REPLACEMENT BATTERIES PART NO. 5098,5135, 5097 is HLJ.

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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

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Related Devices (Code: HLJ)

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.

K131961HEINE BETA 200(R) OPHTHALMOSCOPEHeine Optotechnik GmbH & Co. KGK131719OPHTHALMOSCOPES DIAGNOSTIC INSTRUMENT KITSMedical Devices (Pvt) , Ltd.K123587HEINE MINI 3000 LED OPHTHALMOSCOPEHeine Optotechnik GmbH & Co. KGK093495OTOSCOPE AND OPHTHALMOSCOPE DIAGNOSTIC INSTRUMENT KITSAmerican Diagnostic Corp.K070270PICCOLIGHT E50,PICCOLIGHT E56,EUROLIGHT E10, EUROLIGHT E30, AND EUROLIGHT E36Kirchner & Wilhelm GmbH + Co.KgK05259966 VISION TECH OPHTHALMOSCOPE, MODELS YZ6E, YZ6F, YZ6G, YZ11, YZ11C, YZ11D, YZ25ASuzhou 66 Vision Tech Co., Ltd.

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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