The following data is part of a premarket notification filed by Propper Mfg. Co., Inc. with the FDA for Steamline.
Device ID | K895910 |
510k Number | K895910 |
Device Name: | STEAMLINE |
Classification | Indicator, Physical/chemical Sterilization Process |
Applicant | PROPPER MFG. CO., INC. 3604 SKILLMAN AVE. Long Island City, NY 11101 |
Contact | Platko, Phd |
Correspondent | Platko, Phd PROPPER MFG. CO., INC. 3604 SKILLMAN AVE. Long Island City, NY 11101 |
Product Code | JOJ |
CFR Regulation Number | 880.2800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-10-10 |
Decision Date | 1990-08-22 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
10724995095557 | K895910 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
STEAMLINE 74008707 1633096 Dead/Cancelled |
PROPPER MANUFACTURING CO., INC. 1989-12-07 |
STEAMLINE 71665111 0656526 Dead/Expired |
HOFFMAN BEVERAGE COMPANY 1954-04-23 |