HAND/FOOT 624-208— 510(k) K872604

Substantially Equivalent

National Biological Corp.

FDA 510(k) clearance K872604 for HAND/FOOT 624-208, Substantially Equivalent on 1987-07-24. Applicant: National Biological Corp.. Device class: 2.

Clearance details

Applicant: National Biological Corp.
Product code: Code FTC
Device class: Class 2
Regulation: 21 CFR 878.4630
Advisory panel: General, Plastic Surgery
Date received: 1987-07-02
Decision date: 1987-07-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Twinsburg, OH, US

Download summary PDF View on FDA.gov ↗

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Recalls naming K872604

K-number listed on FDA's recall record

Z-1683-2017 — Hand Foot II, UVB-138. One device per box; device is surrounded by foam inserts inside a corrugated box. For UV phototherapy treatment.Class II·Terminated·National Biological Corp·20170127

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K872604.

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