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FDA 510(k)

EXTERNAL INCONTINENCE CATHETER SET-NON

K-Number: K832108 · 1983-07-18

ApplicantPlasco, Inc.
Decision Date1983-07-18
Product CodeKNX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

EXTERNAL INCONTINENCE CATHETER SET-NON is the device name listed in this FDA 510(k) record. The listed applicant is Plasco, Inc.. It received FDA 510(k) clearance on 1983-07-18 under 510(k) number K832108. 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 EXTERNAL INCONTINENCE CATHETER SET-NON?

EXTERNAL INCONTINENCE CATHETER SET-NON is a medical device that received FDA 510(k) clearance on 1983-07-18. The listed applicant is Plasco, Inc.. The 510(k) number is K832108.

When did EXTERNAL INCONTINENCE CATHETER SET-NON receive FDA 510(k) clearance?

EXTERNAL INCONTINENCE CATHETER SET-NON received FDA 510(k) clearance on 1983-07-18, under 510(k) number K832108.

Who is the listed applicant for EXTERNAL INCONTINENCE CATHETER SET-NON?

The FDA 510(k) record lists Plasco, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXTERNAL INCONTINENCE CATHETER SET-NON?

The FDA product code for EXTERNAL INCONTINENCE CATHETER SET-NON 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 Plasco, Inc. 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 16 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

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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