Home / 510(k) Clearances / K884529

510(k) K884529

MICROAIR FLUIDIZED AIR BED by Gsi Development Co. — Product Code INX

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 18, 1988
Date Received
October 28, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bed, Air Fluidized
Device Class
Class II
Regulation Number
890.5160
Review Panel
PM
Submission Type

Other clearances by Gsi Development Co.

  • K926456 — MICROAIR TURN-Q (March 24, 1993)
  • K914674 — MICROAIR 3500 (November 22, 1991)
  • K893708 — FLUIDIZED AIR BED (June 22, 1989)

Other clearances for product code INX

  • K972176 — HOME CARE BEAD BED (January 16, 1998)
  • K964223 — CLINITRON RITE-HITE (May 28, 1997)
  • K943385 — CLINITRON ELEXIS (February 27, 1995)
  • K942184 — CLINITRON AT HOME AIR FLUIDED THERAPY (February 7, 1995)
  • K931168 — X-20 AIR SUPPORT BED (February 17, 1994)
  • K934689 — LOW AIR LOSS MATTRESS, MODIFICATION (February 2, 1994)
  • K924973 — DYLNAMEDICS A.S.A.P. (October 15, 1993)
  • K926402 — COMFORT CARE LOW AIR LOSS THERAPY BED (March 24, 1993)
  • K924686 — REM-AIR (February 12, 1993)
  • K920112 — CLINITRON C-II (January 24, 1992)