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FDA 510(k)

CATH CONTROL

K-Number: K914211 · 1991-11-22

ApplicantHighpoint Medical Corp.
Decision Date1991-11-22
Product CodeKNY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CATH CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Highpoint Medical Corp.. It received FDA 510(k) clearance on 1991-11-22 under 510(k) number K914211. The device is classified under product code KNY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATH CONTROL?

CATH CONTROL is a medical device that received FDA 510(k) clearance on 1991-11-22. The listed applicant is Highpoint Medical Corp.. The 510(k) number is K914211.

When did CATH CONTROL receive FDA 510(k) clearance?

CATH CONTROL received FDA 510(k) clearance on 1991-11-22, under 510(k) number K914211.

Who is the listed applicant for CATH CONTROL?

The FDA 510(k) record lists Highpoint Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CATH CONTROL?

The FDA product code for CATH CONTROL is KNY.

Related Clinical Trials

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Other records listing Highpoint Medical Corp. 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.

K932300FOG CONTROL, LENS FOG REDUCTION DEVICE

Related Devices (Code: KNY)

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.

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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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