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FDA 510(k)

TOUCH 'N HEAT MODEL 5002, MODIFICATION

K-Number: K915243 · 1992-01-21

ApplicantAnalytic Technology
Decision Date1992-01-21
Product CodeEKM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TOUCH 'N HEAT MODEL 5002, MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Analytic Technology. It received FDA 510(k) clearance on 1992-01-21 under 510(k) number K915243. The device is classified under product code EKM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOUCH 'N HEAT MODEL 5002, MODIFICATION?

TOUCH 'N HEAT MODEL 5002, MODIFICATION is a medical device that received FDA 510(k) clearance on 1992-01-21. The listed applicant is Analytic Technology. The 510(k) number is K915243.

When did TOUCH 'N HEAT MODEL 5002, MODIFICATION receive FDA 510(k) clearance?

TOUCH 'N HEAT MODEL 5002, MODIFICATION received FDA 510(k) clearance on 1992-01-21, under 510(k) number K915243.

Who is the listed applicant for TOUCH 'N HEAT MODEL 5002, MODIFICATION?

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 TOUCH 'N HEAT MODEL 5002, MODIFICATION?

The FDA product code for TOUCH 'N HEAT MODEL 5002, MODIFICATION is EKM.

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Other records listing Analytic Technology 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.

K921604TOUCH N' HEAT, MODIFICATIONK890735COATED APEX PROBEK864500ANALYTIC TECHNOLOGY ENDO ANALYZER MODEL 8001K832179HOT PROBE MODEL 6001K823486TOUCH-N-HEAT MODEL 5001K820598HOT & COLD PULP TESTER #4001

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Related Devices (Code: EKM)

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.

K073369EI DOWNPAK BARRIER SLEEVESHu-Friedy Mfg. Co., Inc.K070246DOWN PAKEndo Twinn B.V.K051573TGP (GUTTA PERCHA CONTAINING TETRACYCLINE OR DOXYCYCLINE)Dr. Howard Martin, P.A.K042870ENDO TWINNEndo Twinn B.V.K023819FIBERFILL SGPPentron Clinical TechnologiesK971641ANTIBACTERIAL GUTTA PERCHADr. Howard Martin, P.A.

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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