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FDA 510(k)

VALVE FOR CLOSED SYS. URINARY DRAINAGE

K-Number: K770399 · 1977-03-09

ApplicantWill Ross Co.
Decision Date1977-03-09
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VALVE FOR CLOSED SYS. URINARY DRAINAGE is the device name listed in this FDA 510(k) record. The listed applicant is Will Ross Co.. It received FDA 510(k) clearance on 1977-03-09 under 510(k) number K770399. The device is classified under product code KNX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VALVE FOR CLOSED SYS. URINARY DRAINAGE?

VALVE FOR CLOSED SYS. URINARY DRAINAGE is a medical device that received FDA 510(k) clearance on 1977-03-09. The listed applicant is Will Ross Co.. The 510(k) number is K770399.

When did VALVE FOR CLOSED SYS. URINARY DRAINAGE receive FDA 510(k) clearance?

VALVE FOR CLOSED SYS. URINARY DRAINAGE received FDA 510(k) clearance on 1977-03-09, under 510(k) number K770399.

Who is the listed applicant for VALVE FOR CLOSED SYS. URINARY DRAINAGE?

The FDA 510(k) record lists Will Ross Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VALVE FOR CLOSED SYS. URINARY DRAINAGE?

The FDA product code for VALVE FOR CLOSED SYS. URINARY DRAINAGE is KNX.

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 Will Ross Co. 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 14 devices →

Related Devices (Code: KNX)

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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