The following data is part of a premarket notification filed by Porges Corp. with the FDA for Porges Sclerotherapy Needles.
| Device ID | K896424 |
| 510k Number | K896424 |
| Device Name: | PORGES SCLEROTHERAPY NEEDLES |
| Classification | Endoscopic Injection Needle, Gastroenterology-urology |
| Applicant | PORGES CORP. 5700 WEST 23RD AVE. Gary, IN 46406 |
| Contact | Harry M Kaufman |
| Correspondent | Harry M Kaufman PORGES CORP. 5700 WEST 23RD AVE. Gary, IN 46406 |
| Product Code | FBK |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-11-08 |
| Decision Date | 1990-01-26 |