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FDA 510(k)

KINETIC MODEL 500

K-Number: K891756 · 1989-04-19

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

Device Summary

KINETIC MODEL 500 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 K891756. The device is classified under product code FSY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KINETIC MODEL 500?

KINETIC MODEL 500 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 K891756.

When did KINETIC MODEL 500 receive FDA 510(k) clearance?

KINETIC MODEL 500 received FDA 510(k) clearance on 1989-04-19, under 510(k) number K891756.

Who is the listed applicant for KINETIC MODEL 500?

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 500?

The FDA product code for KINETIC MODEL 500 is FSY.

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 700K891758KINETIC MODEL 132K891757KINETIC MODEL 1000K891759KINETIC MODEL 330

Related Devices (Code: FSY)

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.

K132747VISUM BLADE LED SURGICAL LIGHTING SYSTEMStryker CommunicationsK132307VIDA LED SURGICAL LIGHTING SYSTEMConvida Healthcare & Systems CorporationK131893AMICO CE SERIES SURGICAL LIGHTS, MIRA LED SERIES MINOR SURGICAL LIGHTSAjw Technology Consultants, Inc.K122875ORICARE L2700Oricare, Inc.K120392CHROMOPHARE F 628 AND F 528Berchtold GmbH & Co. KGK102758TRULIGHT 5520 AND TRULIGHT 5320Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg

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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