FLUIDAIR— 510(k) K881917

Substantially Equivalent

Kinetic Concepts, Inc.

FDA 510(k) clearance K881917 for FLUIDAIR, Substantially Equivalent on 1988-11-14. Applicant: Kinetic Concepts, Inc.. Device class: 2.

Clearance details

Applicant: Kinetic Concepts, Inc.
Product code: Code INX
Device class: Class 2
Regulation: 21 CFR 890.5160
Advisory panel: Physical Medicine
Date received: 1988-05-09
Decision date: 1988-11-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Antonio, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code INX

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K943385 — CLINITRON ELEXIS1995-02-27
K942184 — CLINITRON AT HOME AIR FLUIDED THERAPY1995-02-07
K931168 — X-20 AIR SUPPORT BED1994-02-17

More clearances from Kinetic Concepts, Inc.

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K022011 — V.A.C. ABDOMINAL DRESSING2003-02-26
K021500 — VACUUM ASSISTED CLOSURE2002-12-20

Data sourced from openFDA. This site is unofficial and independent of the FDA.