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FDA 510(k)

KINNET

K-Number: K851875 · 1985-08-22

ApplicantKinetic Concepts, Inc.
Decision Date1985-08-22
Product CodeINY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KINNET is the device name listed in this FDA 510(k) record. The listed applicant is Kinetic Concepts, Inc.. It received FDA 510(k) clearance on 1985-08-22 under 510(k) number K851875. The device is classified under product code INY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KINNET?

KINNET is a medical device that received FDA 510(k) clearance on 1985-08-22. The listed applicant is Kinetic Concepts, Inc.. The 510(k) number is K851875.

When did KINNET receive FDA 510(k) clearance?

KINNET received FDA 510(k) clearance on 1985-08-22, under 510(k) number K851875.

Who is the listed applicant for KINNET?

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

What is the FDA product code for KINNET?

The FDA product code for KINNET is INY.

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Other records listing Kinetic Concepts, 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.

K050261V.A.C. GRANUFOAM SILVER PROTECTION DRESSINGK041642V.A.C. GRANUFOAM SILVER DRESSINGK032310MINI V.A.C., V.A.C. FREEDOM, V.A.C. ATSK022011V.A.C. ABDOMINAL DRESSINGK021500VACUUM ASSISTED CLOSUREK021501V.A.C. INSTILLAMAT (VACUUM ASSISTED CLOSURE INSTILLAMAT

View all 48 devices →

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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