Who is the manufacturer of 'CATCH-IT' OR FECAL CONTAINMENT DEVICE?

Midwest Medical Co. filed the 510(k) submission for 'CATCH-IT' OR FECAL CONTAINMENT DEVICE (K873929).

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

EXB. It is classified under 21 CFR 876.5900 as a Class 1 device in the Gastroenterology, Urology panel.

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

510(k) clearance (submission type: Traditional).

Who can help prepare an FDA 510(k) submission like 'CATCH-IT' OR FECAL CONTAINMENT DEVICE?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

'CATCH-IT' OR FECAL CONTAINMENT DEVICE

K873929 · Midwest Medical Co. · EXB · Dec 3, 1987 · Gastroenterology, Urology

Device Facts

Record ID	K873929
Device Name	'CATCH-IT' OR FECAL CONTAINMENT DEVICE
Applicant	Midwest Medical Co.
Product Code	EXB · Gastroenterology, Urology
Decision Date	Dec 3, 1987
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 876.5900
Device Class	Class 1

Sort by

Ready

Predicate graph will load when search results are available.

Embedding visualization will load when search results are available.

PDF viewer will load when search results are available.

Loading panels...

Select an item from Submissions

Click any panel, subpart, regulation, product code, or device to see details here.

Section Matches

Results will appear here.

Product Code Matches

Results will appear here.

Special Control Matches

Results will appear here.

Loading collections...

'CATCH-IT' OR FECAL CONTAINMENT DEVICE

Device Facts

Panel 1

Section Matches

Product Code Matches

Special Control Matches

My Alerts

'CATCH-IT' OR FECAL CONTAINMENT DEVICE

Device Facts

Panel 1

Section Matches

Product Code Matches

Special Control Matches

My Alerts

Create Alert

Search Filters

Agent Token

Welcome

Check your email

Welcome!