FDA 510(k)

PULPTESTER MODEL 2001

K-Number: K790799 · 1979-05-31

Decision Date1979-05-31

Product CodeEAT

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

PULPTESTER MODEL 2001 is the device name listed in this FDA 510(k) record. The listed applicant is Analytic Technology. It received FDA 510(k) clearance on 1979-05-31 under 510(k) number K790799. 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 PULPTESTER MODEL 2001?

PULPTESTER MODEL 2001 is a medical device that received FDA 510(k) clearance on 1979-05-31. The listed applicant is Analytic Technology. The 510(k) number is K790799.

When did PULPTESTER MODEL 2001 receive FDA 510(k) clearance?

PULPTESTER MODEL 2001 received FDA 510(k) clearance on 1979-05-31, under 510(k) number K790799.

Who is the listed applicant for PULPTESTER MODEL 2001?

The FDA 510(k) record lists Analytic Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PULPTESTER MODEL 2001?

The FDA product code for PULPTESTER MODEL 2001 is EAT.

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Other records listing Analytic Technology as applicant

K921604TOUCH N' HEAT, MODIFICATION K915243TOUCH 'N HEAT MODEL 5002, MODIFICATION K890735COATED APEX PROBE K864500ANALYTIC TECHNOLOGY ENDO ANALYZER MODEL 8001 K832179HOT PROBE MODEL 6001 K823486TOUCH-N-HEAT MODEL 5001

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Related Devices (Code: EAT)

K022097THERMIQUEParkell, Inc.K021298ELEMENTS DIAGNOSTIC UNITSybron Endo/Analytic K012427PHARMAETHYL LOCAL PULP AND VITALITY TESTING AGENTSpecialites Septodont K011666CHILLITHeatshield, Inc.K990225ENDO ANALYZER, MODEL 8005, MODIFIEDSybron Dental Specialties, Inc.K973439ENDO ANALYZER, MODEL 8005Sybron Dental Specialties, Inc.

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.