The following data is part of a premarket notification filed by American Hospital Supply Corp. with the FDA for Aap Dosimetry Release Or Basin Sets.
Device ID | K832826 |
510k Number | K832826 |
Device Name: | AAP DOSIMETRY RELEASE OR BASIN SETS |
Classification | Basin, Emesis |
Applicant | AMERICAN HOSPITAL SUPPLY CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | FNY |
CFR Regulation Number | 880.6730 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1983-08-19 |
Decision Date | 1984-04-23 |