GE LOGIQ A100 MP, MODEL 2272413

System, Imaging, Pulsed Echo, Ultrasonic

GENERAL ELECTRIC CO.

The following data is part of a premarket notification filed by General Electric Co. with the FDA for Ge Logiq A100 Mp, Model 2272413.

Pre-market Notification Details

• Device ID: K012560
• 510k Number: K012560
• Device Name: GE LOGIQ A100 MP, MODEL 2272413
• Classification: System, Imaging, Pulsed Echo, Ultrasonic
• Applicant: GENERAL ELECTRIC CO. P.O. BOX 414 Milwaukee, WI 53201
• Contact: Allen Schuh
• Correspondent: Allen Schuh; GENERAL ELECTRIC CO. P.O. BOX 414 Milwaukee, WI 53201
• Product Code: IYO
• CFR Regulation Number: 892.1560 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Special
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2001-08-08
• Decision Date: 2001-08-23
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00840682117364	K012560	000
00840682117333	K012560	000
00840682117296	K012560	000
00840682117258	K012560	000