The following data is part of a premarket notification filed by Fisher Scientific Co., Llc. with the FDA for Fisher Diagnostics Anaerobic Blood Cult.
Device ID | K792056 |
510k Number | K792056 |
Device Name: | FISHER DIAGNOSTICS ANAEROBIC BLOOD CULT |
Classification | Culture Media, General Nutrient Broth |
Applicant | FISHER SCIENTIFIC CO., LLC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | JSC |
CFR Regulation Number | 866.2350 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1979-10-15 |
Decision Date | 1979-11-16 |