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FDA 510(k)

SUCTION T CONNECTOR

K-Number: K862434 · 1986-07-10

ApplicantAcutronic Medical Systems AG
Decision Date1986-07-10
Product Code
DecisionSubstantially Equivalent

Device Summary

SUCTION T CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Acutronic Medical Systems AG. It received FDA 510(k) clearance on 1986-07-10 under 510(k) number K862434. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUCTION T CONNECTOR?

SUCTION T CONNECTOR is a medical device that received FDA 510(k) clearance on 1986-07-10. The listed applicant is Acutronic Medical Systems AG. The 510(k) number is K862434.

When did SUCTION T CONNECTOR receive FDA 510(k) clearance?

SUCTION T CONNECTOR received FDA 510(k) clearance on 1986-07-10, under 510(k) number K862434.

Who is the listed applicant for SUCTION T CONNECTOR?

The FDA 510(k) record lists Acutronic Medical Systems AG as the applicant. This does not by itself establish the device manufacturer.

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 Acutronic Medical Systems AG 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.

K012691MONSOON CRITICAL CARE JET VENTILATOR AND ACCESSORIESK012693MISTRAL CRITICAL CARE JET VENTILATOR AND ACCESSORIESK936009AMS 3000MK900745VS-200S JET VENTILATORK900744AMS 3000 PORTABLE JET VENTILATORK883865EXTERNAL JET SYNCHRONIZER, MODEL AMS-1010

View all 12 devices →

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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