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FDA 510(k)

CEMENT, RESIN DENTAL (SOLO-TACH)

K-Number: K760376 · 1976-08-23

ApplicantL.D. Caulk Co.
Decision Date1976-08-23
Product CodeDYH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CEMENT, RESIN DENTAL (SOLO-TACH) 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 1976-08-23 under 510(k) number K760376. The device is classified under product code DYH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEMENT, RESIN DENTAL (SOLO-TACH)?

CEMENT, RESIN DENTAL (SOLO-TACH) is a medical device that received FDA 510(k) clearance on 1976-08-23. The listed applicant is L.D. Caulk Co.. The 510(k) number is K760376.

When did CEMENT, RESIN DENTAL (SOLO-TACH) receive FDA 510(k) clearance?

CEMENT, RESIN DENTAL (SOLO-TACH) received FDA 510(k) clearance on 1976-08-23, under 510(k) number K760376.

Who is the listed applicant for CEMENT, RESIN DENTAL (SOLO-TACH)?

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

What is the FDA product code for CEMENT, RESIN DENTAL (SOLO-TACH)?

The FDA product code for CEMENT, RESIN DENTAL (SOLO-TACH) is DYH.

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

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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.

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