The following data is part of a premarket notification filed by Irrimax Corporation with the FDA for Irrisept Antimicrobial Wound Lavage.
Device ID | K222804 |
510k Number | K222804 |
Device Name: | Irrisept Antimicrobial Wound Lavage |
Classification | Lavage, Jet |
Applicant | Irrimax Corporation 1665 Lakes Parkway, Suite 102 Lawrenceville, GA 30043 |
Contact | Tanya Eberle |
Correspondent | Tanya Eberle Irrimax Corporation 1665 Lakes Parkway, Suite 102 Lawrenceville, GA 30043 |
Product Code | FQH |
CFR Regulation Number | 880.5475 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | Yes |
Date Received | 2022-09-16 |
Decision Date | 2022-09-22 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00842351120026 | K222804 | 000 |
00842351120040 | K222804 | 000 |