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FDA 510(k)

AC POWERED AND BATTERY POWERED MEDICAL EXAM. LIGHT

K-Number: K910942 · 1991-06-11

ApplicantMdt Biologic Co.
Decision Date1991-06-11
Product CodeFSS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AC POWERED AND BATTERY POWERED MEDICAL EXAM. LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Mdt Biologic Co.. It received FDA 510(k) clearance on 1991-06-11 under 510(k) number K910942. The device is classified under product code FSS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AC POWERED AND BATTERY POWERED MEDICAL EXAM. LIGHT?

AC POWERED AND BATTERY POWERED MEDICAL EXAM. LIGHT is a medical device that received FDA 510(k) clearance on 1991-06-11. The listed applicant is Mdt Biologic Co.. The 510(k) number is K910942.

When did AC POWERED AND BATTERY POWERED MEDICAL EXAM. LIGHT receive FDA 510(k) clearance?

AC POWERED AND BATTERY POWERED MEDICAL EXAM. LIGHT received FDA 510(k) clearance on 1991-06-11, under 510(k) number K910942.

Who is the listed applicant for AC POWERED AND BATTERY POWERED MEDICAL EXAM. LIGHT?

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

What is the FDA product code for AC POWERED AND BATTERY POWERED MEDICAL EXAM. LIGHT?

The FDA product code for AC POWERED AND BATTERY POWERED MEDICAL EXAM. LIGHT is FSS.

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Other records listing Mdt Biologic 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.

K954736ACCESS (POWERCLAVE)K954940MDT STERIGRIP DISPOSABLE, SOFT COVER, LIGHT HANDLEK943654HARVEY CHEMICLAVE EC5000, EC5500, EC6000 STERILIZERSK911087CASTLE WASHER/DISINFECTOR, MODEL 7550K910777MDT/CASTLE MODELS S-8 TABLE TOP STEAM STERILIZERK910778STEAM VACUUM PULSE STERILIZER SYSTEM (SVPSS)

View all 8 devices →

Related Devices (Code: FSS)

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.

K091246ILED 3 MOBILE (I300M), TRULIGHT 5500 MOBILE (T500M), TRULIGHT 5300 MOBILE (T300M)Trumpf Medizin Systeme GmbH + Co. KGK003489NEXT GENERAL M20 SURGICAL LIGHT; NEXT GENERATION M16 MINOR SURGERY LIGHT; NEXT GENERATION SPOTLIGHT; NEXT GENERATION M8Medical Illumination International, Inc.K984124AESCULAP XENON LIGHT SOURCEAesculap, Inc.K981962CUDA PRODUCTS CORP. MODEL M300 (M-300) LIGHTSOURCECuda Products Co.K981821VES 3001/2 DUAL OUTPUT VIDEO ILLUMINATORAngiolaz, Inc.K981469CERMAX300 LIGHTSOURCECuda Products Co.

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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