The following data is part of a premarket notification filed by Pilling Co. with the FDA for Mehigan-pilling Angioscopic Vascular Instrum. Line.
| Device ID | K911099 |
| 510k Number | K911099 |
| Device Name: | MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE |
| Classification | Stripper, Artery, Intraluminal |
| Applicant | PILLING CO. 420 DELAWARE DR. Fort Washington, PA 19034 |
| Contact | Richard G Jones |
| Correspondent | Richard G Jones PILLING CO. 420 DELAWARE DR. Fort Washington, PA 19034 |
| Product Code | DWX |
| CFR Regulation Number | 870.4875 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-03-12 |
| Decision Date | 1991-06-25 |