The following data is part of a premarket notification filed by Life-tech Intl., Inc. with the FDA for Model 6110 Iontophoretic Applicator.
Device ID | K863166 |
510k Number | K863166 |
Device Name: | MODEL 6110 IONTOPHORETIC APPLICATOR |
Classification | Device, Iontophoresis, Other Uses |
Applicant | LIFE-TECH INTL., INC. P.O. BOX 36221 Houston, TX 77236 -6221 |
Contact | Coats, Md |
Correspondent | Coats, Md LIFE-TECH INTL., INC. P.O. BOX 36221 Houston, TX 77236 -6221 |
Product Code | EGJ |
CFR Regulation Number | 890.5525 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-08-18 |
Decision Date | 1987-03-04 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00702173155920 | K863166 | 000 |