IMPAK ACRYLIC REPAIR RESIN LIQUID— 510(k) K033020

Substantially Equivalent

Cmp Industries, LLC

FDA 510(k) clearance K033020 for IMPAK ACRYLIC REPAIR RESIN LIQUID, Substantially Equivalent on 2003-12-19. Applicant: Cmp Industries, LLC. Device class: 2.

Clearance details

Applicant
Cmp Industries, LLC
Product code
Code EBI
Device class
Class 2
Regulation
21 CFR 872.3760
Advisory panel
Dental
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Albany, NY, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code EBI

view all

More clearances from Cmp Industries, LLC

view all

Adverse events under product code EBI

product code EBI
Other
1
Total
1

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recalls naming K033020

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K033020.

Data sourced from openFDA. This site is unofficial and independent of the FDA.