The following data is part of a premarket notification filed by Kuraray Medical Inc. with the FDA for Panavia Sa Cement Handmix Value Pack (universal (a2), White) Panavia Sa Cement Handmix (universal (a2), White) Panavia S.
Device ID | K120378 |
510k Number | K120378 |
Device Name: | PANAVIA SA CEMENT HANDMIX VALUE PACK (UNIVERSAL (A2), WHITE) PANAVIA SA CEMENT HANDMIX (UNIVERSAL (A2), WHITE) PANAVIA S |
Classification | Cement, Dental |
Applicant | KURARAY MEDICAL INC. OTE CENTER BLDG. 7F, 1-1-3, OTEMACHI Chiyoda-ku, JP 100-0004 |
Contact | Michio Takigawa |
Correspondent | Michio Takigawa KURARAY MEDICAL INC. OTE CENTER BLDG. 7F, 1-1-3, OTEMACHI Chiyoda-ku, JP 100-0004 |
Product Code | EMA |
CFR Regulation Number | 872.3275 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-02-07 |
Decision Date | 2012-03-30 |
Summary: | summary |