The following data is part of a premarket notification filed by Bio/data Corp. with the FDA for Microsample Coagulation Analyser Model 110p.
Device ID | K854546 |
510k Number | K854546 |
Device Name: | MICROSAMPLE COAGULATION ANALYSER MODEL 110P |
Classification | System, Multipurpose For In Vitro Coagulation Studies |
Applicant | BIO/DATA CORP. 3615 DAVISVILLE RD. P.O. BOX 250 Hatboro, PA 19040 |
Contact | James Eichelberger |
Correspondent | James Eichelberger BIO/DATA CORP. 3615 DAVISVILLE RD. P.O. BOX 250 Hatboro, PA 19040 |
Product Code | JPA |
CFR Regulation Number | 864.5425 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-11-13 |
Decision Date | 1986-01-07 |