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FDA 510(k)

'CATCH-IT' OR FECAL CONTAINMENT DEVICE

K-Number: K873929 · 1987-12-03

Decision Date1987-12-03
Product CodeEXB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

'CATCH-IT' OR FECAL CONTAINMENT DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Midwest Medical Co.. It received FDA 510(k) clearance on 1987-12-03 under 510(k) number K873929. The device is classified under product code EXB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 'CATCH-IT' OR FECAL CONTAINMENT DEVICE?

'CATCH-IT' OR FECAL CONTAINMENT DEVICE is a medical device that received FDA 510(k) clearance on 1987-12-03. The listed applicant is Midwest Medical Co.. The 510(k) number is K873929.

When did 'CATCH-IT' OR FECAL CONTAINMENT DEVICE receive FDA 510(k) clearance?

'CATCH-IT' OR FECAL CONTAINMENT DEVICE received FDA 510(k) clearance on 1987-12-03, under 510(k) number K873929.

Who is the listed applicant for 'CATCH-IT' OR FECAL CONTAINMENT DEVICE?

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

What is the FDA product code for 'CATCH-IT' OR FECAL CONTAINMENT DEVICE?

The FDA product code for 'CATCH-IT' OR FECAL CONTAINMENT DEVICE is EXB.

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.

Related Devices (Code: EXB)

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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