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510(k) K910709

WEEVAC TC HAND CARRIED RESCUE STRETCHER by W. Murphy Ent., Inc. — Product Code FPP

K910709 is an FDA 510(k) premarket notification submitted by W. Murphy Ent., Inc. for the device "WEEVAC TC HAND CARRIED RESCUE STRETCHER". The FDA issued a decision of Substantially Equivalent on April 1, 1991. The device falls under product code FPP (Stretcher, Hand-Carried), a Class I device regulated under 21 CFR 880.6900. W. Murphy Ent., Inc. has at least 2 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 1, 1991
Date Received
February 20, 1991
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 by W. Murphy Ent., Inc.

  • K902474 — WEEVAC 1 PORTABLE RESCUE STRETCHER (July 24, 1990)
  • K902521 — WEEVAC 6 INFANT EVACUATION STRETCHER (June 22, 1990)

Other clearances for product code FPP

  • K030283 — BABY POD (April 22, 2003)
  • K942356 — MED-EVAC-4 MEDICAL EVACUATION STRETCHER (July 19, 1994)
  • 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)

FDA data resources