The following data is part of a premarket notification filed by Ventrex Laboratories, Inc. with the FDA for Ventrex Ip Specific E Enzyme Immunoassay.
Device ID | K870624 |
510k Number | K870624 |
Device Name: | VENTREX IP SPECIFIC E ENZYME IMMUNOASSAY |
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 | 1987-02-13 |
Decision Date | 1987-03-24 |