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FDA 510(k)

KINETIC MODEL 330

K-Number: K891759 · 1989-04-19

ApplicantKinetic Biomedical Services, Inc.
Decision Date1989-04-19
Product CodeFSS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KINETIC MODEL 330 is the device name listed in this FDA 510(k) record. The listed applicant is Kinetic Biomedical Services, Inc.. It received FDA 510(k) clearance on 1989-04-19 under 510(k) number K891759. 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 KINETIC MODEL 330?

KINETIC MODEL 330 is a medical device that received FDA 510(k) clearance on 1989-04-19. The listed applicant is Kinetic Biomedical Services, Inc.. The 510(k) number is K891759.

When did KINETIC MODEL 330 receive FDA 510(k) clearance?

KINETIC MODEL 330 received FDA 510(k) clearance on 1989-04-19, under 510(k) number K891759.

Who is the listed applicant for KINETIC MODEL 330?

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

What is the FDA product code for KINETIC MODEL 330?

The FDA product code for KINETIC MODEL 330 is FSS.

Related Clinical Trials

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.

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Other records listing Kinetic Biomedical Services, 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.

K892808KINETIC MODEL 700K891756KINETIC MODEL 500K891758KINETIC MODEL 132K891757KINETIC MODEL 1000

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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