The following data is part of a premarket notification filed by Medical Specialties, Inc. with the FDA for Msi Hematology Control +.
Device ID | K871067 |
510k Number | K871067 |
Device Name: | MSI HEMATOLOGY CONTROL + |
Classification | Mixture, Hematology Quality Control |
Applicant | MEDICAL SPECIALTIES, INC. 3610 KENNEDY RD. South Plainfield, NJ 07080 |
Contact | Ronald Devita |
Correspondent | Ronald Devita MEDICAL SPECIALTIES, INC. 3610 KENNEDY RD. South Plainfield, NJ 07080 |
Product Code | JPK |
CFR Regulation Number | 864.8625 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-03-18 |
Decision Date | 1987-03-25 |