PRENATAL WEDGE— 510(k) K895343

Substantially Equivalent

Kay Ent.

FDA 510(k) clearance K895343 for PRENATAL WEDGE, Substantially Equivalent on 1989-09-29. Applicant: Kay Ent.. Device class: 2.

Clearance details

Applicant: Kay Ent.
Product code: Code JFB
Device class: Class 2
Regulation: 21 CFR 890.5880
Advisory panel: Physical Medicine
Date received: 1989-09-01
Decision date: 1989-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tucson, AZ, US

Download summary PDF View on FDA.gov ↗

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