PROPLATE

Electrosurgical, Cutting & Coagulation & Accessories

BIO PROTECH, INC.

The following data is part of a premarket notification filed by Bio Protech, Inc. with the FDA for Proplate.

Pre-market Notification Details

• Device ID: K073360
• 510k Number: K073360
• Device Name: PROPLATE
• Classification: Electrosurgical, Cutting & Coagulation & Accessories
• Applicant: BIO PROTECH, INC. 1676 VILLAGE GREEN SUITE A Crofton, MD 21114
• Contact: E.j. Smith
• Correspondent: Jeff Rongero; UNDERWRITERS LABORATORIES, INC. 12 LABORATORY DR. Research Triangle, NC 27709
• Product Code: GEI
• CFR Regulation Number: 878.4400 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: Yes
• Combination Product: No
• Date Received: 2007-11-30
• Decision Date: 2007-12-19
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
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20817325020972	K073360	000
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