MULTIBLAST MEDIUM
Media, Reproductive
IRVINE SCIENTIFIC SALES CO., INC.
The following data is part of a premarket notification filed by Irvine Scientific Sales Co., Inc. with the FDA for Multiblast Medium.
Pre-market Notification Details
| Device ID | K034063 |
| 510k Number | K034063 |
| Device Name: | MULTIBLAST MEDIUM |
| Classification | Media, Reproductive |
| Applicant | IRVINE SCIENTIFIC SALES CO., INC. 2511 DAIMLER ST. Santa Ana, CA 92705 |
| Contact | Wendell Lee |
| Correspondent | Wendell Lee IRVINE SCIENTIFIC SALES CO., INC. 2511 DAIMLER ST. Santa Ana, CA 92705 |
| Product Code | MQL |
| CFR Regulation Number | 884.6180 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-12-31 |
| Decision Date | 2004-04-26 |
| Summary: | summary |
NIH GUDID Devices
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00893727002293 | K034063 | 000 |
Trademark Results [MULTIBLAST MEDIUM]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MULTIBLAST MEDIUM 78309250 3165930 Live/Registered |
FUJIFILM IRVINE SCIENTIFIC, INC. 2003-10-03 |
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