The following data is part of a premarket notification filed by Labeltape Meditect, Inc. with the FDA for Spect.e.n.s. Repositionable, Pin Type, Tens.
Device ID | K894042 |
510k Number | K894042 |
Device Name: | SPECT.E.N.S. REPOSITIONABLE, PIN TYPE, TENS |
Classification | Electrode, Cutaneous |
Applicant | LABELTAPE MEDITECT, INC. 4275 AIRWEST DR., S.E. P.O. BOX 8823 Grand Rapids, MI 49508 |
Contact | Lora Jones |
Correspondent | Lora Jones LABELTAPE MEDITECT, INC. 4275 AIRWEST DR., S.E. P.O. BOX 8823 Grand Rapids, MI 49508 |
Product Code | GXY |
CFR Regulation Number | 882.1320 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-06-06 |
Decision Date | 1989-08-11 |