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FDA 510(k)

DISPOSABLE PARALLEL Y CONNECTORS

K-Number: K802541 · 1981-01-16

ApplicantTexas Medical Products, Inc.
Decision Date1981-01-16
Product CodeKRI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE PARALLEL Y CONNECTORS is the device name listed in this FDA 510(k) record. The listed applicant is Texas Medical Products, Inc.. It received FDA 510(k) clearance on 1981-01-16 under 510(k) number K802541. The device is classified under product code KRI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE PARALLEL Y CONNECTORS?

DISPOSABLE PARALLEL Y CONNECTORS is a medical device that received FDA 510(k) clearance on 1981-01-16. The listed applicant is Texas Medical Products, Inc.. The 510(k) number is K802541.

When did DISPOSABLE PARALLEL Y CONNECTORS receive FDA 510(k) clearance?

DISPOSABLE PARALLEL Y CONNECTORS received FDA 510(k) clearance on 1981-01-16, under 510(k) number K802541.

Who is the listed applicant for DISPOSABLE PARALLEL Y CONNECTORS?

The FDA 510(k) record lists Texas Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE PARALLEL Y CONNECTORS?

The FDA product code for DISPOSABLE PARALLEL Y CONNECTORS is KRI.

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Other records listing Texas Medical Products, Inc. as applicant

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Related Devices (Code: KRI)

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.

K0203653TM MYOCARDIAL NEEDLE-TEMPERATURE PROBE3t Medical Systems, LLCK992635INTERFACE MODULE IDDDStoeckert InstrumenteK990512STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTSStoeckert InstrumenteK934782AMMEX TUBING ORGANIZERAmmex Cardiopulmonary Corp.K926233CARDIO2 CYCLEErgometrix, Inc.K922404TUBE GRIPGeorgia Medical Products, 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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