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FDA 510(k)

THERMAL PULP TESTER

K-Number: K940260 · 1994-03-07

Decision Date1994-03-07
Product CodeEAT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

THERMAL PULP TESTER is the device name listed in this FDA 510(k) record. The listed applicant is Union Broach, Div. Moyco Industries, Inc.. It received FDA 510(k) clearance on 1994-03-07 under 510(k) number K940260. The device is classified under product code EAT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERMAL PULP TESTER?

THERMAL PULP TESTER is a medical device that received FDA 510(k) clearance on 1994-03-07. The listed applicant is Union Broach, Div. Moyco Industries, Inc.. The 510(k) number is K940260.

When did THERMAL PULP TESTER receive FDA 510(k) clearance?

THERMAL PULP TESTER received FDA 510(k) clearance on 1994-03-07, under 510(k) number K940260.

Who is the listed applicant for THERMAL PULP TESTER?

The FDA 510(k) record lists Union Broach, Div. Moyco Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THERMAL PULP TESTER?

The FDA product code for THERMAL PULP TESTER is EAT.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Union Broach, Div. Moyco Industries, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 14 devices →

Related Devices (Code: EAT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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