LUSTRALLOY— 510(k) K820738

Substantially Equivalent

Hoyt Laboratories

FDA 510(k) clearance K820738 for LUSTRALLOY, Substantially Equivalent on 1982-04-09. Applicant: Hoyt Laboratories. Device class: 2.

Clearance details

Applicant: Hoyt Laboratories
Product code: Code EJJ
Device class: Class 2
Regulation: 21 CFR 872.3070
Advisory panel: Dental
Date received: 1982-03-18
Decision date: 1982-04-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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More clearances from Hoyt Laboratories

K811154 — HOYT ECONO-TRAY1981-05-13
K810830 — HOYT COTTON ROLLS1981-04-14
K780834 — PREVI DENT PROPHYLAXIS MINT NDC1978-06-02
K771881 — REPLICA BONDING AGENT1977-11-09
K771880 — REPLICA DENTAL COMPOSIT1977-10-20

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