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FDA 510(k)

TEXAS INTERFACE PRESSURE EVALUATOR-TIPE

K-Number: K831800 · 1983-08-16

ApplicantTee-Kay Applied Technology
Decision Date1983-08-16
Product CodeJFC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TEXAS INTERFACE PRESSURE EVALUATOR-TIPE is the device name listed in this FDA 510(k) record. The listed applicant is Tee-Kay Applied Technology. It received FDA 510(k) clearance on 1983-08-16 under 510(k) number K831800. The device is classified under product code JFC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEXAS INTERFACE PRESSURE EVALUATOR-TIPE?

TEXAS INTERFACE PRESSURE EVALUATOR-TIPE is a medical device that received FDA 510(k) clearance on 1983-08-16. The listed applicant is Tee-Kay Applied Technology. The 510(k) number is K831800.

When did TEXAS INTERFACE PRESSURE EVALUATOR-TIPE receive FDA 510(k) clearance?

TEXAS INTERFACE PRESSURE EVALUATOR-TIPE received FDA 510(k) clearance on 1983-08-16, under 510(k) number K831800.

Who is the listed applicant for TEXAS INTERFACE PRESSURE EVALUATOR-TIPE?

The FDA 510(k) record lists Tee-Kay Applied Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TEXAS INTERFACE PRESSURE EVALUATOR-TIPE?

The FDA product code for TEXAS INTERFACE PRESSURE EVALUATOR-TIPE is JFC.

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Related Devices (Code: JFC)

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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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