FDA 510(k)

COMPOSITE RESTORATIVE

K-Number: K802262 · 1980-09-16

Decision Date1980-09-16

Product Code

DecisionUnknown

Device Summary

COMPOSITE RESTORATIVE is the device name listed in this FDA 510(k) record. The listed applicant is L.D. Caulk Co.. It received FDA 510(k) clearance on 1980-09-16 under 510(k) number K802262. FDA Decision: Unknown.

Frequently Asked Questions

What is the COMPOSITE RESTORATIVE?

COMPOSITE RESTORATIVE is a medical device that received FDA 510(k) clearance on 1980-09-16. The listed applicant is L.D. Caulk Co.. The 510(k) number is K802262.

When did COMPOSITE RESTORATIVE receive FDA 510(k) clearance?

COMPOSITE RESTORATIVE received FDA 510(k) clearance on 1980-09-16, under 510(k) number K802262.

Who is the listed applicant for COMPOSITE RESTORATIVE?

The FDA 510(k) record lists L.D. Caulk Co. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing L.D. Caulk Co. as applicant

K801690VALIANT K790585FINESSE K790586CHEMBOND K780560DENTAL AMALGAMATOR K780384IMPROVED DYCAL K780301CAULK TYLOK

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.