The following data is part of a premarket notification filed by Ormed Mfg., Inc. with the FDA for Safety Pins & Rubber Bands.
Device ID | K831915 |
510k Number | K831915 |
Device Name: | SAFETY PINS & RUBBER BANDS |
Classification | Instrument, Surgical, Disposable |
Applicant | ORMED MFG., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | KDC |
CFR Regulation Number | 878.4800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1983-06-14 |
Decision Date | 1983-09-12 |