Cleared Traditional

K802262 - COMPOSITE RESTORATIVE
(FDA 510(k) Clearance)

K802262 · L.D. Caulk Co. · Dental device
Sep 1980
Decision
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Days
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Risk

K802262 is an FDA 510(k) clearance for the COMPOSITE RESTORATIVE..

Submitted by L.D. Caulk Co. (Mchenry, US). The FDA issued a Cleared decision on September 16, 1980.

This device falls under the Dental FDA review panel.

Submission Details

510(k) Number K802262 FDA.gov
FDA Decision Cleared Substantially Equivalent - Product Development Protocol (SESP)
Date Received September 16, 1980
Decision Date September 16, 1980
Days to Decision —
Submission Type Traditional
Review Panel Dental (DE)
Summary —

Device Classification

Product Code —
Device Class —