The following data is part of a premarket notification filed by Intermedics, Inc. with the FDA for Adaptaid(tm) Adapter Sleeve Model 366-33.
Device ID | K894718 |
510k Number | K894718 |
Device Name: | ADAPTAID(TM) ADAPTER SLEEVE MODEL 366-33 |
Classification | Pacemaker Lead Adaptor |
Applicant | INTERMEDICS, INC. P.O. BOX 617 Freeport, TX 77541 -0617 |
Contact | James S Miller |
Correspondent | James S Miller INTERMEDICS, INC. P.O. BOX 617 Freeport, TX 77541 -0617 |
Product Code | DTD |
CFR Regulation Number | 870.3620 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-07-25 |
Decision Date | 1989-09-05 |