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FDA 510(k)

TYCOS DIAGNOSTIC PENLIGHT

K-Number: K760972 · 1977-01-26

ApplicantTaylor Instrument Analytics Co.
Decision Date1977-01-26
Product CodeKYT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TYCOS DIAGNOSTIC PENLIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Taylor Instrument Analytics Co.. It received FDA 510(k) clearance on 1977-01-26 under 510(k) number K760972. The device is classified under product code KYT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TYCOS DIAGNOSTIC PENLIGHT?

TYCOS DIAGNOSTIC PENLIGHT is a medical device that received FDA 510(k) clearance on 1977-01-26. The listed applicant is Taylor Instrument Analytics Co.. The 510(k) number is K760972.

When did TYCOS DIAGNOSTIC PENLIGHT receive FDA 510(k) clearance?

TYCOS DIAGNOSTIC PENLIGHT received FDA 510(k) clearance on 1977-01-26, under 510(k) number K760972.

Who is the listed applicant for TYCOS DIAGNOSTIC PENLIGHT?

The FDA 510(k) record lists Taylor Instrument Analytics Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TYCOS DIAGNOSTIC PENLIGHT?

The FDA product code for TYCOS DIAGNOSTIC PENLIGHT is KYT.

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.

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Other records listing Taylor Instrument Analytics Co. 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.

K780448TRANSPORTABLE OXYGEN PURITY ANALYZER

Related Devices (Code: KYT)

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.

K920782OLYMPIC TRANS-LITEOlympic Medical Corp.K841589C-LITESuncoast Medical Manufacturers, Inc.K841588SUN-LITE WHITE SPOTSuncoast Medical Manufacturers, Inc.K791001PENLIGHT/SWAB HOLDERConcept, Inc.K781228PENLIGHTSAbco Dealers, 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.

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