Home / 510(k) Clearances / K942356

510(k) K942356

MED-EVAC-4 MEDICAL EVACUATION STRETCHER by Montery Bay Corp. — Product Code FPP

K942356 is an FDA 510(k) premarket notification submitted by Montery Bay Corp. for the device "MED-EVAC-4 MEDICAL EVACUATION STRETCHER". The FDA issued a decision of Substantially Equivalent on July 19, 1994. The device falls under product code FPP (Stretcher, Hand-Carried), a Class I device regulated under 21 CFR 880.6900.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 19, 1994
Date Received
May 17, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stretcher, Hand-Carried
Device Class
Class I
Regulation Number
880.6900
Review Panel
HO
Submission Type

Other clearances for product code FPP

  • K030283 — BABY POD (April 22, 2003)
  • K940130 — STRYKER MODEL 6110 EMERGENCY/POLE STRETCHER (March 10, 1994)
  • K940245 — EVACU-SLED (February 28, 1994)
  • K924275 — RESTRAINING STRETCHER (July 27, 1993)
  • K922816 — U P CUSTOM DESIGN, INC. COT EQUIPMENT CARRIER (July 13, 1993)
  • K924669 — FERNO-WASHINGTON BASKET STRETCHER, MODEL 71-W (April 29, 1993)
  • K920805 — LIFE LITE EMERGENCY STRETCHER (May 22, 1992)
  • K915874 — BASKET LITTER CARRIER (May 13, 1992)
  • K914140 — GRASSI GASTROJEJUN TUBE GASTRIC DECOMP/JEJUN FEED (March 31, 1992)
  • K913520 — EVACU SLED (December 4, 1991)

FDA data resources