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FDA 510(k)

TAYLOR & TYCOS ACOUSTIC SPHYGMOMANOMETER

K-Number: K820135 · 1982-03-01

ApplicantSybron Corp.
Decision Date1982-03-01
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TAYLOR & TYCOS ACOUSTIC SPHYGMOMANOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Corp.. It received FDA 510(k) clearance on 1982-03-01 under 510(k) number K820135. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAYLOR & TYCOS ACOUSTIC SPHYGMOMANOMETER?

TAYLOR & TYCOS ACOUSTIC SPHYGMOMANOMETER is a medical device that received FDA 510(k) clearance on 1982-03-01. The listed applicant is Sybron Corp.. The 510(k) number is K820135.

When did TAYLOR & TYCOS ACOUSTIC SPHYGMOMANOMETER receive FDA 510(k) clearance?

TAYLOR & TYCOS ACOUSTIC SPHYGMOMANOMETER received FDA 510(k) clearance on 1982-03-01, under 510(k) number K820135.

Who is the listed applicant for TAYLOR & TYCOS ACOUSTIC SPHYGMOMANOMETER?

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 TAYLOR & TYCOS ACOUSTIC SPHYGMOMANOMETER?

The FDA product code for TAYLOR & TYCOS ACOUSTIC SPHYGMOMANOMETER is DXN.

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Other records listing Sybron Corp. as applicant

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Related Devices (Code: DXN)

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

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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