LEE-ALLOY DISPOSABLE CAPSULES— 510(k) K780966

Name: FDA 510(k) clearance K780966
Creator: U.S. Food and Drug Administration
Published: 1978-08-21

Substantially Equivalent

Lee Pharmaceuticals

FDA 510(k) clearance K780966 for LEE-ALLOY DISPOSABLE CAPSULES, Substantially Equivalent on 1978-08-21. Applicant: Lee Pharmaceuticals. Device class: 1.

Clearance details

Applicant: Lee Pharmaceuticals
Product code: Code DZS
Device class: Class 1
Regulation: 21 CFR 872.3110
Advisory panel: Dental
Date received: 1978-06-12
Decision date: 1978-08-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DZS

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K822610 — PRECAPSULED DENTAL AMALGAM1982-09-14
K802967 — DISPERSALLOY-DISPERSED PHASE ALLOY SELF-1980-12-30
K781243 — MERCURY DISP. CAPSULE1978-09-20

More clearances from Lee Pharmaceuticals

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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

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