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FDA 510(k)

TEMPTRONIC 100 WATER BATH

K-Number: K792060 · 1979-12-04

ApplicantSybron Corp.
Decision Date1979-12-04
Product CodeJTQ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TEMPTRONIC 100 WATER BATH is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Corp.. It received FDA 510(k) clearance on 1979-12-04 under 510(k) number K792060. The device is classified under product code JTQ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMPTRONIC 100 WATER BATH?

TEMPTRONIC 100 WATER BATH is a medical device that received FDA 510(k) clearance on 1979-12-04. The listed applicant is Sybron Corp.. The 510(k) number is K792060.

When did TEMPTRONIC 100 WATER BATH receive FDA 510(k) clearance?

TEMPTRONIC 100 WATER BATH received FDA 510(k) clearance on 1979-12-04, under 510(k) number K792060.

Who is the listed applicant for TEMPTRONIC 100 WATER BATH?

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

What is the FDA product code for TEMPTRONIC 100 WATER BATH?

The FDA product code for TEMPTRONIC 100 WATER BATH is JTQ.

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 Sybron Corp. 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 37 devices →

Related Devices (Code: JTQ)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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