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FDA 510(k)

NEEDLELESS URINE SAMPLING PORT

K-Number: K944236 · 1994-11-16

Decision Date1994-11-16
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NEEDLELESS URINE SAMPLING PORT 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 1994-11-16 under 510(k) number K944236. 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 NEEDLELESS URINE SAMPLING PORT?

NEEDLELESS URINE SAMPLING PORT is a medical device that received FDA 510(k) clearance on 1994-11-16. The listed applicant is Kendall Healthcare Products Co. Div.Of Tyco Health. The 510(k) number is K944236.

When did NEEDLELESS URINE SAMPLING PORT receive FDA 510(k) clearance?

NEEDLELESS URINE SAMPLING PORT received FDA 510(k) clearance on 1994-11-16, under 510(k) number K944236.

Who is the listed applicant for NEEDLELESS URINE SAMPLING PORT?

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 NEEDLELESS URINE SAMPLING PORT?

The FDA product code for NEEDLELESS URINE SAMPLING PORT 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 Kendall Healthcare Products Co. Div.Of Tyco Health 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 66 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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