The following data is part of a premarket notification filed by Stan-pak Ent. with the FDA for Specialist Cast Padding.
Device ID | K820155 |
510k Number | K820155 |
Device Name: | SPECIALIST CAST PADDING |
Classification | Bandage, Cast |
Applicant | STAN-PAK ENT. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | ITG |
CFR Regulation Number | 890.3025 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1982-01-19 |
Decision Date | 1982-02-12 |