METRICIDE

Sterilant, Medical Devices

METREX RESEARCH CORP.

The following data is part of a premarket notification filed by Metrex Research Corp. with the FDA for Metricide.

Pre-market Notification Details

• Device ID: K930284
• 510k Number: K930284
• Device Name: METRICIDE
• Classification: Sterilant, Medical Devices
• Applicant: METREX RESEARCH CORP. P.O. BOX 646 10270 SOUTH PROGRESS WAY Parker, CO 80134
• Contact: Vera Buffaloe
• Correspondent: Vera Buffaloe; METREX RESEARCH CORP. P.O. BOX 646 10270 SOUTH PROGRESS WAY Parker, CO 80134
• Product Code: MED
• CFR Regulation Number: 880.6885 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1993-01-19
• Decision Date: 1994-12-06

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00304040003947	K930284	000
H97110140522	K930284	000
H9711014002	K930284	000