The following data is part of a premarket notification filed by Richard-allan Medical Ind., Inc. with the FDA for Reflex(tm) Clip Applier.
Device ID | K862404 |
510k Number | K862404 |
Device Name: | REFLEX(TM) CLIP APPLIER |
Classification | Clip, Implantable |
Applicant | RICHARD-ALLAN MEDICAL IND., INC. 8850 M89 BOX 351 Richland, MI 49083 |
Contact | Julie Powell |
Correspondent | Julie Powell RICHARD-ALLAN MEDICAL IND., INC. 8850 M89 BOX 351 Richland, MI 49083 |
Product Code | FZP |
CFR Regulation Number | 878.4300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-06-25 |
Decision Date | 1986-07-23 |