HEAD & FOOT END DROP PEDI-CRIB— 510(k) K925817

Substantially Equivalent

Pedicraft, Inc.

FDA 510(k) clearance K925817 for HEAD & FOOT END DROP PEDI-CRIB, Substantially Equivalent on 1993-04-20. Applicant: Pedicraft, Inc.. Device class: 2.

Clearance details

Applicant: Pedicraft, Inc.
Product code: Code FMS
Device class: Class 2
Regulation: 21 CFR 880.5140
Advisory panel: General Hospital
Date received: 1992-11-17
Decision date: 1993-04-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FMS

K970334 — NATURE'S CRADLE1997-04-25
K963210 — VAIL 100 PEDIATRIC CRIB1996-11-13
K960747 — NATURE'S CRADLE MODEL C15001996-05-22
K960012 — STRYKER ADEL BASSINET1996-03-25
K951024 — NATURE'S CRADLE1995-06-05

More clearances from Pedicraft, Inc.

K925949 — PEDICRAGT BASSINET1993-04-20
K905629 — PEDICRAFT INFANT REFLUX WEDGE1991-03-13
K905630 — INFANT REFLUX SLING1991-03-13
K821773 — PEDICRAFT BED, MODEL B29441982-06-23

Data sourced from openFDA. This site is unofficial and independent of the FDA.