MERCURY DISP. CAPSULE— 510(k) K781243

Substantially Equivalent

Lee Pharmaceuticals

FDA 510(k) clearance K781243 for MERCURY DISP. CAPSULE, Substantially Equivalent on 1978-09-20. 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: 1978-09-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DZS

K822610 — PRECAPSULED DENTAL AMALGAM1982-09-14
K802967 — DISPERSALLOY-DISPERSED PHASE ALLOY SELF-1980-12-30
K780966 — LEE-ALLOY DISPOSABLE CAPSULES1978-08-21

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.