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FDA 510(k)

URINARY LEG BAG, STEOILE

K-Number: K771435 · 1977-09-20

Decision Date1977-09-20
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

URINARY LEG BAG, STEOILE is the device name listed in this FDA 510(k) record. The listed applicant is Meddev International Corp.. It received FDA 510(k) clearance on 1977-09-20 under 510(k) number K771435. 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 URINARY LEG BAG, STEOILE?

URINARY LEG BAG, STEOILE is a medical device that received FDA 510(k) clearance on 1977-09-20. The listed applicant is Meddev International Corp.. The 510(k) number is K771435.

When did URINARY LEG BAG, STEOILE receive FDA 510(k) clearance?

URINARY LEG BAG, STEOILE received FDA 510(k) clearance on 1977-09-20, under 510(k) number K771435.

Who is the listed applicant for URINARY LEG BAG, STEOILE?

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

What is the FDA product code for URINARY LEG BAG, STEOILE?

The FDA product code for URINARY LEG BAG, STEOILE 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 Meddev International 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.

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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