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FDA 510(k)

IONESCU-SHILEY COMPOSITE CONDUIT-PULMONI

K-Number: K790425 · 1979-03-28

ApplicantShiley, Inc.
Decision Date1979-03-28
Product Code
DecisionSubstantially Equivalent

Device Summary

IONESCU-SHILEY COMPOSITE CONDUIT-PULMONI is the device name listed in this FDA 510(k) record. The listed applicant is Shiley, Inc.. It received FDA 510(k) clearance on 1979-03-28 under 510(k) number K790425. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IONESCU-SHILEY COMPOSITE CONDUIT-PULMONI?

IONESCU-SHILEY COMPOSITE CONDUIT-PULMONI is a medical device that received FDA 510(k) clearance on 1979-03-28. The listed applicant is Shiley, Inc.. The 510(k) number is K790425.

When did IONESCU-SHILEY COMPOSITE CONDUIT-PULMONI receive FDA 510(k) clearance?

IONESCU-SHILEY COMPOSITE CONDUIT-PULMONI received FDA 510(k) clearance on 1979-03-28, under 510(k) number K790425.

Who is the listed applicant for IONESCU-SHILEY COMPOSITE CONDUIT-PULMONI?

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

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Other records listing Shiley, 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.

K920594SHILEY PERFUSION TUBING SETSK910991SHILEY THERAPEUTIC AUTOTRANSFUSION SYSTEMK911876SHILEY PLEXUS(R) VENOUS RESERVOIR, PVR1200K910923BCD ADVANCEDK901548BIOMEDICAL SENSORS-SHILEY BGM 4000 INTRA BLOOD GASK903435SHILEY SPECIALIZED TRACHEOSTOMY TUBE

View all 174 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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