SWITCHBLADE

Electrosurgical, Cutting & Coagulation & Accessories

SNOWDEN PENCER, INC.

The following data is part of a premarket notification filed by Snowden Pencer, Inc. with the FDA for Switchblade.

Pre-market Notification Details

• Device ID: K030890
• 510k Number: K030890
• Device Name: SWITCHBLADE
• Classification: Electrosurgical, Cutting & Coagulation & Accessories
• Applicant: SNOWDEN PENCER, INC. 5175 SOUTH ROYAL ATLANTA DR. Tucker, GA 30084 -3053
• Contact: David J Booth
• Product Code: GEI
• CFR Regulation Number: 878.4400 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: Yes
• Combination Product: No
• Date Received: 2003-03-21
• Decision Date: 2003-04-04
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
20885403141895	K030890	000
20885403141888	K030890	000
20885403156271	K030890	000
20885403141871	K030890	000
20885403141710	K030890	000
20885403141864	K030890	000
20885403187459	K030890	000