Visible Light Cure Calcium Hydroxide Liner

FDA 510(k) K884949 · Ortho Source

Substantially Equivalent

510(k) numberK884949

Submission

Device name
Visible Light Cure Calcium Hydroxide Liner
Applicant
Ortho Source
North Hollywood, CA, US
Received
November 25, 1988
Decision date
February 23, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
EJK – Liner, Cavity, Calcium Hydroxide
Device class
Class II (moderate risk)
Regulation
21 CFR 872.3250
Specialty
Dental

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Questions and answers

When was Visible Light Cure Calcium Hydroxide Liner cleared by the FDA?

Visible Light Cure Calcium Hydroxide Liner (K884949) received a 510(k) decision of Substantially Equivalent on February 23, 1989, 90 days after the submission was received.

What is the product code of K884949?

The FDA product code is EJK – Liner, Cavity, Calcium Hydroxide, a Class II (moderate risk) device regulated under 21 CFR 872.3250.