PARA-PAK
Iodine, Grams
MERIDIAN DIAGNOSTICS, INC.
The following data is part of a premarket notification filed by Meridian Diagnostics, Inc. with the FDA for Para-pak.
Pre-market Notification Details
| Device ID | K811722 |
| 510k Number | K811722 |
| Device Name: | PARA-PAK |
| Classification | Iodine, Grams |
| Applicant | MERIDIAN DIAGNOSTICS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HYI |
| CFR Regulation Number | 864.1850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-06-18 |
| Decision Date | 1981-07-15 |
Trademark Results [PARA-PAK]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PARA-PAK 74446009 1856525 Live/Registered |
MERIDIAN BIOSCIENCE, INC. 1993-10-12 |
 PARA-PAK 73572589 1426358 Dead/Cancelled |
ALCAN ALUMINUM CORPORATION 1985-12-09 |
 PARA-PAK 73415638 1280647 Dead/Cancelled |
Triton Industries, Ltd. 1983-03-03 |
 PARA-PAK 73212665 not registered Dead/Abandoned |
Meridian Diagnostics, Inc. 1979-04-23 |
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