Who is the manufacturer of ODOR-END EMERGENCY CLEAN UP POWDER?

Cdc Products Corp. filed the 510(k) submission for ODOR-END EMERGENCY CLEAN UP POWDER (K882878).

What is the FDA product code for ODOR-END EMERGENCY CLEAN UP POWDER?

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 ODOR-END EMERGENCY CLEAN UP POWDER?

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

Who can help prepare an FDA 510(k) submission like ODOR-END EMERGENCY CLEAN UP POWDER?

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.

ODOR-END EMERGENCY CLEAN UP POWDER

K882878 · Cdc Products Corp. · EXB · Dec 8, 1988 · Gastroenterology, Urology

Device Facts

Record ID	K882878
Device Name	ODOR-END EMERGENCY CLEAN UP POWDER
Applicant	Cdc Products Corp.
Product Code	EXB · Gastroenterology, Urology
Decision Date	Dec 8, 1988
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 876.5900
Device Class	Class 1

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