EVERLIFE

Electrode, Cutaneous

EVERLIFE MEDICAL INSTRUMENT CO., LTD.

The following data is part of a premarket notification filed by Everlife Medical Instrument Co., Ltd. with the FDA for Everlife.

Pre-market Notification Details

• Device ID: K050788
• 510k Number: K050788
• Device Name: EVERLIFE
• Classification: Electrode, Cutaneous
• Applicant: EVERLIFE MEDICAL INSTRUMENT CO., LTD. NO. 58, FU-CHIUN ST. Hsin-chu City, TW 300
• Contact: Jen Ke-min
• Correspondent: Jen Ke-min; EVERLIFE MEDICAL INSTRUMENT CO., LTD. NO. 58, FU-CHIUN ST. Hsin-chu City, TW 300
• Product Code: GXY
• CFR Regulation Number: 882.1320 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2005-03-28
• Decision Date: 2005-05-13
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00858688006926	K050788	000
00858688006599	K050788	000
00858688006582	K050788	000
00858688006568	K050788	000
00858688006551	K050788	000
00858688006315	K050788	000
00858688006278	K050788	000
00858688006162	K050788	000
00858688006148	K050788	000
00858688006131	K050788	000
00858688006124	K050788	000
00858688006063	K050788	000
00858688006605	K050788	000
00858688006612	K050788	000
00858688006629	K050788	000
00858688006919	K050788	000
00858688006902	K050788	000
00858688006803	K050788	000
00858688006766	K050788	000
00858688006728	K050788	000
00858688006711	K050788	000
00858688006698	K050788	000
00858688006681	K050788	000
00858688006674	K050788	000
00858688006650	K050788	000
00858688006643	K050788	000
00858688006056	K050788	000