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FDA 510(k)

MS401097-17,MS722-K,MS720,MS721,MS722

K-Number: K962767 · 1997-07-03

ApplicantAlexander Mfg. Co.
Decision Date1997-07-03
Product CodeHLJ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MS401097-17,MS722-K,MS720,MS721,MS722 is the device name listed in this FDA 510(k) record. The listed applicant is Alexander Mfg. Co.. It received FDA 510(k) clearance on 1997-07-03 under 510(k) number K962767. 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 MS401097-17,MS722-K,MS720,MS721,MS722?

MS401097-17,MS722-K,MS720,MS721,MS722 is a medical device that received FDA 510(k) clearance on 1997-07-03. The listed applicant is Alexander Mfg. Co.. The 510(k) number is K962767.

When did MS401097-17,MS722-K,MS720,MS721,MS722 receive FDA 510(k) clearance?

MS401097-17,MS722-K,MS720,MS721,MS722 received FDA 510(k) clearance on 1997-07-03, under 510(k) number K962767.

Who is the listed applicant for MS401097-17,MS722-K,MS720,MS721,MS722?

The FDA 510(k) record lists Alexander Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MS401097-17,MS722-K,MS720,MS721,MS722?

The FDA product code for MS401097-17,MS722-K,MS720,MS721,MS722 is HLJ.

Other records listing Alexander Mfg. Co. 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.

K982896ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER LP9K981776ALEXANDER MANUFACTURING CO. BATTERY PART NUMBER MC146XK981728ALEXANDER MANUFACTURING CO. BATTERY PART NUMBER H134K980224ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS822K974061RECHARGEABLE BATTERY PART NUMBER GL825-200K973851ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY #M12/630

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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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