PEDICRAFT INFANT REFLUX WEDGE— 510(k) K905629

Substantially Equivalent

Pedicraft, Inc.

FDA 510(k) clearance K905629 for PEDICRAFT INFANT REFLUX WEDGE, Substantially Equivalent on 1991-03-13. Applicant: Pedicraft, Inc.. Device class: 1.

Clearance details

Applicant: Pedicraft, Inc.
Product code: Code FRP
Device class: Class 1
Regulation: 21 CFR 880.5680
Advisory panel: General Hospital
Date received: 1990-12-14
Decision date: 1991-03-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Pedicraft, Inc.

K925817 — HEAD & FOOT END DROP PEDI-CRIB1993-04-20
K925949 — PEDICRAGT BASSINET1993-04-20
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.