The following data is part of a premarket notification filed by Jayco Pharmaceuticals with the FDA for Polyp-saver Sleve.
Device ID | K840800 |
510k Number | K840800 |
Device Name: | POLYP-SAVER SLEVE |
Classification | Endoscopic Grasping/cutting Instrument, Non-powered |
Applicant | JAYCO PHARMACEUTICALS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | OCZ |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-02-23 |
Decision Date | 1984-03-23 |