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FDA 510(k)

AESCULAP XENON LIGHT SOURCE

K-Number: K984124 · 1999-02-01

ApplicantAesculap, Inc.
Decision Date1999-02-01
Product CodeFSS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AESCULAP XENON LIGHT SOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 1999-02-01 under 510(k) number K984124. 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 AESCULAP XENON LIGHT SOURCE?

AESCULAP XENON LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 1999-02-01. The listed applicant is Aesculap, Inc.. The 510(k) number is K984124.

When did AESCULAP XENON LIGHT SOURCE receive FDA 510(k) clearance?

AESCULAP XENON LIGHT SOURCE received FDA 510(k) clearance on 1999-02-01, under 510(k) number K984124.

Who is the listed applicant for AESCULAP XENON LIGHT SOURCE?

The FDA 510(k) record lists Aesculap, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AESCULAP XENON LIGHT SOURCE?

The FDA product code for AESCULAP XENON LIGHT SOURCE is FSS.

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Other records listing Aesculap, Inc. as applicant

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K242762Aesculap Aicon® Series Container SystemK242003XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter SetK223596SQ.line KERRISONK214041Aesculap AICON ContainerK211572Aesculap Slim Clip ApplierK203739ELAN 4 Electro Motor System

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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.K981962CUDA PRODUCTS CORP. MODEL M300 (M-300) LIGHTSOURCECuda Products Co.K981821VES 3001/2 DUAL OUTPUT VIDEO ILLUMINATORAngiolaz, Inc.K981469CERMAX300 LIGHTSOURCECuda Products Co.K980044XENON 300MXPerkinelmer Optoelectronics

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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