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FDA 510(k)

SOLID STATE CONTINUOUS FLOW CONTROL MODEL W/K101

K-Number: K861460 · 1986-05-02

Decision Date1986-05-02
Product CodeLJK
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SOLID STATE CONTINUOUS FLOW CONTROL MODEL W/K101 is the device name listed in this FDA 510(k) record. The listed applicant is Widran Urological Group, Ltd.. It received FDA 510(k) clearance on 1986-05-02 under 510(k) number K861460. The device is classified under product code LJK. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLID STATE CONTINUOUS FLOW CONTROL MODEL W/K101?

SOLID STATE CONTINUOUS FLOW CONTROL MODEL W/K101 is a medical device that received FDA 510(k) clearance on 1986-05-02. The listed applicant is Widran Urological Group, Ltd.. The 510(k) number is K861460.

When did SOLID STATE CONTINUOUS FLOW CONTROL MODEL W/K101 receive FDA 510(k) clearance?

SOLID STATE CONTINUOUS FLOW CONTROL MODEL W/K101 received FDA 510(k) clearance on 1986-05-02, under 510(k) number K861460.

Who is the listed applicant for SOLID STATE CONTINUOUS FLOW CONTROL MODEL W/K101?

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

What is the FDA product code for SOLID STATE CONTINUOUS FLOW CONTROL MODEL W/K101?

The FDA product code for SOLID STATE CONTINUOUS FLOW CONTROL MODEL W/K101 is LJK.

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 Widran Urological Group, 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.

Related Devices (Code: LJK)

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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