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FDA 510(k)

TOUCH N' HEAT, MODIFICATION

K-Number: K921604 · 1992-08-24

ApplicantAnalytic Technology
Decision Date1992-08-24
Product CodeEKZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TOUCH N' HEAT, 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 1992-08-24 under 510(k) number K921604. The device is classified under product code EKZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOUCH N' HEAT, MODIFICATION?

TOUCH N' HEAT, MODIFICATION is a medical device that received FDA 510(k) clearance on 1992-08-24. The listed applicant is Analytic Technology. The 510(k) number is K921604.

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

TOUCH N' HEAT, MODIFICATION received FDA 510(k) clearance on 1992-08-24, under 510(k) number K921604.

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

The FDA product code for TOUCH N' HEAT, MODIFICATION is EKZ.

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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.

K915243TOUCH 'N HEAT MODEL 5002, 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: EKZ)

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.

K213477Root ZX3J. Morita USA, Inc.K071632PERFECT TISSUE CONTOURING SYSTEM IIColtene/Whaledent, Inc.K063468THE FUGO BLADE FOR DENTISTRYMedisurg , Ltd.K052622MACAN MODEL MC-4A DENTAL ELECTROSURGICAL UNITMacan Engineering Co.K050735MC6AMacan Engineering Co.K023672X O ODONTOSURGE 4Xo Care A/S

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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