510(k) K802317

COMFORT CUSHION DRY BURN PADS, STERILE by American Convertors Div., American Pharmaseal — Product Code KKX

K802317 is an FDA 510(k) premarket notification submitted by American Convertors Div., American Pharmaseal for the device "COMFORT CUSHION DRY BURN PADS, STERILE". The FDA issued a decision of Substantially Equivalent on October 31, 1980. The device falls under product code KKX (Drape, Surgical, Antimicrobial), a Class II device regulated under 21 CFR 878.4370. American Convertors Div., American Pharmaseal has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 31, 1980
Date Received
September 23, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Drape, Surgical, Antimicrobial
Device Class
Class II
Regulation Number
878.4370
Review Panel
HO
Submission Type

Surgical drapes with an antimicrobial agent are subject to 510(k) review, under the procedures established by the 21st Century Cures Act. This product code is the class II non-exempt counterpart of PUI.