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FDA 510(k)

MODIFIED AIR FLUIDIZED BED, KINAIR

K-Number: K880340 · 1988-02-16

ApplicantKinetic Concepts, Inc.
Decision Date1988-02-16
Product CodeINX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODIFIED AIR FLUIDIZED BED, KINAIR 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 1988-02-16 under 510(k) number K880340. The device is classified under product code INX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED AIR FLUIDIZED BED, KINAIR?

MODIFIED AIR FLUIDIZED BED, KINAIR is a medical device that received FDA 510(k) clearance on 1988-02-16. The listed applicant is Kinetic Concepts, Inc.. The 510(k) number is K880340.

When did MODIFIED AIR FLUIDIZED BED, KINAIR receive FDA 510(k) clearance?

MODIFIED AIR FLUIDIZED BED, KINAIR received FDA 510(k) clearance on 1988-02-16, under 510(k) number K880340.

Who is the listed applicant for MODIFIED AIR FLUIDIZED BED, KINAIR?

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 MODIFIED AIR FLUIDIZED BED, KINAIR?

The FDA product code for MODIFIED AIR FLUIDIZED BED, KINAIR is INX.

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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

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Related Devices (Code: INX)

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.

K972176HOME CARE BEAD BEDKinetic Concepts, Inc.K964223CLINITRON RITE-HITEHill-Rom, Inc.K943385CLINITRON ELEXISSsi Medical Services, Inc.K942184CLINITRON AT HOME AIR FLUIDED THERAPYSsi Medical Services, Inc.K931168X-20 AIR SUPPORT BEDAmerican Life Support Technology, Inc.K934689LOW AIR LOSS MATTRESS, MODIFICATIONCardio Systems, Inc.

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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