The following data is part of a premarket notification filed by Acumedia Manufacturers, Inc. with the FDA for W-l Differential Medium.
Device ID | K881574 |
510k Number | K881574 |
Device Name: | W-L DIFFERENTIAL MEDIUM |
Classification | Culture Media, Selective And Non-differential |
Applicant | ACUMEDIA MANUFACTURERS, INC. 3651 CLIPPER MILL RD. Baltimore, MD 21211 |
Contact | Cunningham, Phd |
Correspondent | Cunningham, Phd ACUMEDIA MANUFACTURERS, INC. 3651 CLIPPER MILL RD. Baltimore, MD 21211 |
Product Code | JSJ |
CFR Regulation Number | 866.2360 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-04-11 |
Decision Date | 1988-04-18 |