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510(k) K871475

SOLOLIFT - PATIENT TRANSFER STRETCHER by Adel Medical , Ltd. — Product Code FMR

K871475 is an FDA 510(k) premarket notification submitted by Adel Medical , Ltd. for the device "SOLOLIFT - PATIENT TRANSFER STRETCHER". The FDA issued a decision of Substantially Equivalent on May 11, 1987. The device falls under product code FMR (Device, Transfer, Patient, Manual), a Class I device regulated under 21 CFR 880.6785. Adel Medical , Ltd. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 11, 1987
Date Received
April 14, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Transfer, Patient, Manual
Device Class
Class I
Regulation Number
880.6785
Review Panel
HO
Submission Type

Other clearances by Adel Medical , Ltd.

  • K890476 — ADEL - MODEL 986 INFANT WARMER (June 16, 1989)
  • K874610 — ADEL MODEL 2100 BIRTHING BED (January 21, 1988)
  • K861030 — LABOR-DELIVERY STRETCH/BED (April 23, 1986)
  • K860020 — MINOR SURGERY LIGHT MODEL 2112 (January 24, 1986)
  • K833321 — LABOR/DELIVERY/RECOVERY BED LDR-600 (November 14, 1983)
  • K810886 — ADEL MEDICAL BIRTHING BED, #LD-500 (April 23, 1981)
  • K801622 — ADEL MEDICAL BIRTHING BED, MOD. LD-400 (August 14, 1980)

Other clearances for product code FMR

  • K801796 — THE COMFORT LIFT (August 13, 1980)
  • K800373 — TENDERLIFT (March 12, 1980)
  • K792318 — SKIL-CARE TURN AND HOLD PAD (December 20, 1979)
  • K770499 — PATIENT TURNING AND REPOSITIONING G DEV. (April 29, 1977)

FDA data resources