The following data is part of a premarket notification filed by Immuno-mycologics, Inc. with the FDA for Histoplasma Mycelial #cf10020x.
Device ID | K791394 |
510k Number | K791394 |
Device Name: | HISTOPLASMA MYCELIAL #CF10020X |
Classification | Antigens, Histoplasma Capsulatum, All |
Applicant | IMMUNO-MYCOLOGICS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | GMJ |
CFR Regulation Number | 866.3320 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1979-07-11 |
Decision Date | 1979-08-16 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00816387020346 | K791394 | 000 |
00816387020339 | K791394 | 000 |