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FDA 510(k)

TS-301 THREE-WAY PULP TESTER

K-Number: K800138 · 1980-02-13

ApplicantTamler-Stoneham Instruments
Decision Date1980-02-13
Product CodeEAT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TS-301 THREE-WAY PULP TESTER is the device name listed in this FDA 510(k) record. The listed applicant is Tamler-Stoneham Instruments. It received FDA 510(k) clearance on 1980-02-13 under 510(k) number K800138. 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 TS-301 THREE-WAY PULP TESTER?

TS-301 THREE-WAY PULP TESTER is a medical device that received FDA 510(k) clearance on 1980-02-13. The listed applicant is Tamler-Stoneham Instruments. The 510(k) number is K800138.

When did TS-301 THREE-WAY PULP TESTER receive FDA 510(k) clearance?

TS-301 THREE-WAY PULP TESTER received FDA 510(k) clearance on 1980-02-13, under 510(k) number K800138.

Who is the listed applicant for TS-301 THREE-WAY PULP TESTER?

The FDA 510(k) record lists Tamler-Stoneham Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TS-301 THREE-WAY PULP TESTER?

The FDA product code for TS-301 THREE-WAY PULP TESTER is EAT.

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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.

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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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