APOLLO AIR FLUIDIZED BED— 510(k) K842987

Substantially Equivalent

Apollo Fluid Dynamics

FDA 510(k) clearance K842987 for APOLLO AIR FLUIDIZED BED, Substantially Equivalent on 1984-08-02. Applicant: Apollo Fluid Dynamics. Device class: 2.

Clearance details

Applicant: Apollo Fluid Dynamics
Product code: Code INX
Device class: Class 2
Regulation: 21 CFR 890.5160
Advisory panel: Physical Medicine
Date received: 1984-07-30
Decision date: 1984-08-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code INX

K972176 — HOME CARE BEAD BED1998-01-16
K964223 — CLINITRON RITE-HITE1997-05-28
K943385 — CLINITRON ELEXIS1995-02-27
K942184 — CLINITRON AT HOME AIR FLUIDED THERAPY1995-02-07
K931168 — X-20 AIR SUPPORT BED1994-02-17

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