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FDA 510(k)

TRACHEAL SUCTION CATHETER

K-Number: K935600 · 1994-05-10

Decision Date1994-05-10
Product CodeBSY
Advisory CommitteeAN
DecisionUnknown

Device Summary

TRACHEAL SUCTION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Puritas Health Care, Inc.. It received FDA 510(k) clearance on 1994-05-10 under 510(k) number K935600. The device is classified under product code BSY. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the TRACHEAL SUCTION CATHETER?

TRACHEAL SUCTION CATHETER is a medical device that received FDA 510(k) clearance on 1994-05-10. The listed applicant is Puritas Health Care, Inc.. The 510(k) number is K935600.

When did TRACHEAL SUCTION CATHETER receive FDA 510(k) clearance?

TRACHEAL SUCTION CATHETER received FDA 510(k) clearance on 1994-05-10, under 510(k) number K935600.

Who is the listed applicant for TRACHEAL SUCTION CATHETER?

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

What is the FDA product code for TRACHEAL SUCTION CATHETER?

The FDA product code for TRACHEAL SUCTION CATHETER is BSY.

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.

Other records listing Puritas Health Care, 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.

View all 24 devices →

Related Devices (Code: BSY)

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.

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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