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FDA 510(k)

TYCOS SELF-CHECK/DIGITAL FEVER THERMO

K-Number: K842132 · 1984-07-18

ApplicantSybron Corp.
Decision Date1984-07-18
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TYCOS SELF-CHECK/DIGITAL FEVER THERMO is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Corp.. It received FDA 510(k) clearance on 1984-07-18 under 510(k) number K842132. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TYCOS SELF-CHECK/DIGITAL FEVER THERMO?

TYCOS SELF-CHECK/DIGITAL FEVER THERMO is a medical device that received FDA 510(k) clearance on 1984-07-18. The listed applicant is Sybron Corp.. The 510(k) number is K842132.

When did TYCOS SELF-CHECK/DIGITAL FEVER THERMO receive FDA 510(k) clearance?

TYCOS SELF-CHECK/DIGITAL FEVER THERMO received FDA 510(k) clearance on 1984-07-18, under 510(k) number K842132.

Who is the listed applicant for TYCOS SELF-CHECK/DIGITAL FEVER THERMO?

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 TYCOS SELF-CHECK/DIGITAL FEVER THERMO?

The FDA product code for TYCOS SELF-CHECK/DIGITAL FEVER THERMO is FLL.

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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.

K862284SEALITEK854855PROOF ALGINATE IMPRESSION MATERIALK844092DIAGNOSTIC MICROSOPCE SLIDESK841910KERR SEALAPEX ROOT CANAL SEALERK841732LIEBEL-FLARSHEIM AFC 1000 X-RAY FILMK840469TYCOS SELF CHECK BPM3 BLOOD PRESS MONI

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Related Devices (Code: FLL)

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

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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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