LEE COMPOSITE INLAY SYSTEM— 510(k) K873123

Substantially Equivalent

Lee Pharmaceuticals

FDA 510(k) clearance K873123 for LEE COMPOSITE INLAY SYSTEM, Substantially Equivalent on 1988-01-20. Applicant: Lee Pharmaceuticals. Device class: 2.

Clearance details

Applicant: Lee Pharmaceuticals
Product code: Code EBF
Device class: Class 2
Regulation: 21 CFR 872.3690
Advisory panel: Dental
Date received: 1987-08-10
Decision date: 1988-01-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: South El Monte, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Lee Pharmaceuticals

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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.