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FDA 510(k)

MTS CATHETER ADAPTER FOR GUIDANCE ENTRY

K-Number: K791797 · 1979-10-11

ApplicantMedical Testing System, Inc.
Decision Date1979-10-11
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MTS CATHETER ADAPTER FOR GUIDANCE ENTRY is the device name listed in this FDA 510(k) record. The listed applicant is Medical Testing System, Inc.. It received FDA 510(k) clearance on 1979-10-11 under 510(k) number K791797. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MTS CATHETER ADAPTER FOR GUIDANCE ENTRY?

MTS CATHETER ADAPTER FOR GUIDANCE ENTRY is a medical device that received FDA 510(k) clearance on 1979-10-11. The listed applicant is Medical Testing System, Inc.. The 510(k) number is K791797.

When did MTS CATHETER ADAPTER FOR GUIDANCE ENTRY receive FDA 510(k) clearance?

MTS CATHETER ADAPTER FOR GUIDANCE ENTRY received FDA 510(k) clearance on 1979-10-11, under 510(k) number K791797.

Who is the listed applicant for MTS CATHETER ADAPTER FOR GUIDANCE ENTRY?

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

What is the FDA product code for MTS CATHETER ADAPTER FOR GUIDANCE ENTRY?

The FDA product code for MTS CATHETER ADAPTER FOR GUIDANCE ENTRY is DTL.

Related Clinical Trials

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Other records listing Medical Testing System, Inc. 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.

K801802ELECTROMAGNETIC BLOOD & ARTERIAL GAUGEK801799ATRIAL/VENTRICULAR SEQENTIAL #080-20000K801800UNIVERSAL TEMP. PACING ELECT. #080-10000K770641MINI-CONER TM

Related Devices (Code: DTL)

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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