The following data is part of a premarket notification filed by Terumo Medical Corp. with the FDA for Terumo Dental Needles.
Device ID | K864970 |
510k Number | K864970 |
Device Name: | TERUMO DENTAL NEEDLES |
Classification | Needle, Dental |
Applicant | TERUMO MEDICAL CORP. 125 BLUE BALL RD. Elkton, MD 21921 |
Contact | Harald Jacoby |
Correspondent | Harald Jacoby TERUMO MEDICAL CORP. 125 BLUE BALL RD. Elkton, MD 21921 |
Product Code | DZM |
CFR Regulation Number | 872.4730 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-12-22 |
Decision Date | 1987-03-10 |