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FDA 510(k)

CURITY(R) PERCUTANEOUS CATHETERS

K-Number: K895972 · 1990-03-13

ApplicantKendall Healthcare Products Co. Div.Of Tyco Health
Decision Date1990-03-13
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CURITY(R) PERCUTANEOUS CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. It received FDA 510(k) clearance on 1990-03-13 under 510(k) number K895972. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURITY(R) PERCUTANEOUS CATHETERS?

CURITY(R) PERCUTANEOUS CATHETERS is a medical device that received FDA 510(k) clearance on 1990-03-13. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. The 510(k) number is K895972.

When did CURITY(R) PERCUTANEOUS CATHETERS receive FDA 510(k) clearance?

CURITY(R) PERCUTANEOUS CATHETERS received FDA 510(k) clearance on 1990-03-13, under 510(k) number K895972.

Who is the listed applicant for CURITY(R) PERCUTANEOUS CATHETERS?

The FDA 510(k) record lists Kendall Healthcare Products Co. Div.Of Tyco Health as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CURITY(R) PERCUTANEOUS CATHETERS?

The FDA product code for CURITY(R) PERCUTANEOUS CATHETERS is DQY.

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Other records listing Kendall Healthcare Products Co. Div.Of Tyco Health as applicant

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Related Devices (Code: DQY)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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