The following data is part of a premarket notification filed by Ventrex Laboratories, Inc. with the FDA for Turbo-rast Specific Ige Assay.
Device ID | K904330 |
510k Number | K904330 |
Device Name: | TURBO-RAST SPECIFIC IGE ASSAY |
Classification | System, Test, Radioallergosorbent (rast) Immunological |
Applicant | VENTREX LABORATORIES, INC. 217 READ ST. P.O. BOX 9731 Portland, ME 04103 |
Contact | James W Champlin |
Correspondent | James W Champlin VENTREX LABORATORIES, INC. 217 READ ST. P.O. BOX 9731 Portland, ME 04103 |
Product Code | DHB |
CFR Regulation Number | 866.5750 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-09-20 |
Decision Date | 1990-12-07 |