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FDA 510(k)

SCHNEIDER MONORAIL-PMC PRESSURE MONITORING CATH.

K-Number: K896741 · 1990-02-28

Decision Date1990-02-28
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SCHNEIDER MONORAIL-PMC PRESSURE MONITORING CATH. is the device name listed in this FDA 510(k) record. The listed applicant is Schneider Intl., Ltd.. It received FDA 510(k) clearance on 1990-02-28 under 510(k) number K896741. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCHNEIDER MONORAIL-PMC PRESSURE MONITORING CATH.?

SCHNEIDER MONORAIL-PMC PRESSURE MONITORING CATH. is a medical device that received FDA 510(k) clearance on 1990-02-28. The listed applicant is Schneider Intl., Ltd.. The 510(k) number is K896741.

When did SCHNEIDER MONORAIL-PMC PRESSURE MONITORING CATH. receive FDA 510(k) clearance?

SCHNEIDER MONORAIL-PMC PRESSURE MONITORING CATH. received FDA 510(k) clearance on 1990-02-28, under 510(k) number K896741.

Who is the listed applicant for SCHNEIDER MONORAIL-PMC PRESSURE MONITORING CATH.?

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

What is the FDA product code for SCHNEIDER MONORAIL-PMC PRESSURE MONITORING CATH.?

The FDA product code for SCHNEIDER MONORAIL-PMC PRESSURE MONITORING CATH. is DQO.

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 Schneider Intl., Ltd. 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 22 devices →

Related Devices (Code: DQO)

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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