VAPOCIDE

Sterilant, Medical Devices

COTTRELL, LTD.

The following data is part of a premarket notification filed by Cottrell, Ltd. with the FDA for Vapocide.

Pre-market Notification Details

• Device ID: K970726
• 510k Number: K970726
• Device Name: VAPOCIDE
• Classification: Sterilant, Medical Devices
• Applicant: COTTRELL, LTD. 49 PLAIN ST. North Attleboro, MA 02760 -4153
• Contact: Mary Mc Namara-cullinane
• Correspondent: Mary Mc Namara-cullinane; COTTRELL, LTD. 49 PLAIN ST. North Attleboro, MA 02760 -4153
• Product Code: MED
• CFR Regulation Number: 880.6885 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1997-02-28
• Decision Date: 1998-05-18
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
H816VC3381	K970726	000
H816MVC3381	K970726	000