The following data is part of a premarket notification filed by Pmt, Inc. with the FDA for Luo Currettes #3211.
Device ID | K831119 |
510k Number | K831119 |
Device Name: | LUO CURRETTES #3211 |
Classification | Curette, Surgical, General Use |
Applicant | PMT, Inc. Box 464 Hopkins, MN 55343 |
Contact | Alfred A Iversen |
Correspondent | Alfred A Iversen PMT, Inc. Box 464 Hopkins, MN 55343 |
Product Code | FZS |
CFR Regulation Number | 878.4800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1983-04-05 |
Decision Date | 1983-05-09 |