The following data is part of a premarket notification filed by Porges Corp. with the FDA for Porges Cytology Brushes.
Device ID | K896425 |
510k Number | K896425 |
Device Name: | PORGES CYTOLOGY BRUSHES |
Classification | Endoscopic Cytology Brush |
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 | FDX |
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 | 1990-01-29 |