LEE-ALLOY— 510(k) K780967

Substantially Equivalent

Lee Pharmaceuticals

FDA 510(k) clearance K780967 for LEE-ALLOY, Substantially Equivalent on 1978-06-22. Applicant: Lee Pharmaceuticals. Device class: 2.

Clearance details

Applicant: Lee Pharmaceuticals
Product code: Code EJJ
Device class: Class 2
Regulation: 21 CFR 872.3070
Advisory panel: Dental
Date received: 1978-06-12
Decision date: 1978-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EJJ

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K051010 — SECURALLOY, SEPTALLOY NG 50 AND SEPTALLOY NG 702005-05-02
K033434 — BESTALOY2003-11-12
K032152 — BENCO ADMIX2003-08-06
K031658 — BENCO SPHERICAL2003-07-29

More clearances from Lee Pharmaceuticals

K924378 — RESTOBOND 41993-03-31
K912256 — PRECISE(R) BETA QUARTZ GLASS-CERAMIC INSERT1991-07-24
K900809 — LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS1990-06-28
K894315 — RESTOBOND 3/DENTIN-ENAMEL BONDING AGENT1989-10-31
K881903 — PROSTHODENT VL1988-07-01

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