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510(k) K901763

NATURE'S CRADLE(TM) by Infant Advantage, Inc. — Product Code FMS

K901763 is an FDA 510(k) premarket notification submitted by Infant Advantage, Inc. for the device "NATURE'S CRADLE(TM)". The FDA issued a decision of Substantially Equivalent on March 22, 1991. The device falls under product code FMS (Bed, Pediatric Open Hospital), a Class II device regulated under 21 CFR 880.5140. Infant Advantage, Inc. has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 22, 1991
Date Received
April 18, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bed, Pediatric Open Hospital
Device Class
Class II
Regulation Number
880.5140
Review Panel
HO
Submission Type

Other clearances by Infant Advantage, Inc.

  • K970334 — NATURE'S CRADLE (April 25, 1997)
  • K960747 — NATURE'S CRADLE MODEL C1500 (May 22, 1996)
  • K951024 — NATURE'S CRADLE (June 5, 1995)
  • K921327 — NATURE'S CRADLE HM-10 (December 29, 1992)

Other clearances for product code FMS

  • K970334 — NATURE'S CRADLE (April 25, 1997)
  • K963210 — VAIL 100 PEDIATRIC CRIB (November 13, 1996)
  • K960747 — NATURE'S CRADLE MODEL C1500 (May 22, 1996)
  • K960012 — STRYKER ADEL BASSINET (March 25, 1996)
  • K951024 — NATURE'S CRADLE (June 5, 1995)
  • K950051 — BREWER COMPANY TEDDY CRIB MODEL 71900-A, B, 71910-A, B (February 10, 1995)
  • K950058 — MC HEALTHCARE #CH31 CHILD'S CRIB (February 10, 1995)
  • K950059 — MC INFANT CARE UNIE #PP30 (February 10, 1995)
  • K925530 — INSTRUMENT WARMER (June 18, 1993)
  • K925949 — PEDICRAGT BASSINET (April 20, 1993)

FDA data resources