The following data is part of a premarket notification filed by Ormed Gmbh with the FDA for Artocool-s Water Circulating Cold Pack.
Device ID | K964354 |
510k Number | K964354 |
Device Name: | ARTOCOOL-S WATER CIRCULATING COLD PACK |
Classification | Pack, Hot Or Cold, Water Circulating |
Applicant | ORMED GMBH 1000 BURNETTE AVE., SUITE 450 Concord, CA 94520 |
Contact | David W Schlerf |
Correspondent | David W Schlerf ORMED GMBH 1000 BURNETTE AVE., SUITE 450 Concord, CA 94520 |
Product Code | ILO |
CFR Regulation Number | 890.5720 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-10-31 |
Decision Date | 1997-08-29 |
Summary: | summary |