The following data is part of a premarket notification filed by Direct Solutions with the FDA for Hemocue Glucotrol.
Device ID | K964053 |
510k Number | K964053 |
Device Name: | HEMOCUE GLUCOTROL |
Classification | Single (specified) Analyte Controls (assayed And Unassayed) |
Applicant | DIRECT SOLUTIONS 7 HAYRICK LN. P.O. BOX 900 Westford, MA 01886 |
Contact | Bill Donohue |
Correspondent | Bill Donohue DIRECT SOLUTIONS 7 HAYRICK LN. P.O. BOX 900 Westford, MA 01886 |
Product Code | JJX |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-09-30 |
Decision Date | 1996-11-01 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
08718734960935 | K964053 | 000 |
08718734960591 | K964053 | 000 |
08718734960577 | K964053 | 000 |
08718734960560 | K964053 | 000 |