Composite Restorative

FDA 510(k) K802262 · L.D. Caulk Co.

Unknown

510(k) numberK802262

Submission

Device name
Composite Restorative
Applicant
L.D. Caulk Co.
Mchenry, IL, US
Received
September 16, 1980
Decision date
September 16, 1980
Decision
Unknown (SESP)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

More from L.D. Caulk Co.

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K780560Dental AmalgamatorEFD · Traditional 04/21/1978SE
K780384Improved DycalEJK · Traditional 03/15/1978SE
K780301Caulk TylokEMA · Traditional 02/28/1978SE
K771402Nuva-Cote (Modification to)EBC · Traditional 08/26/1977SE
K771399Lip & Cheek RetractorEIG · Traditional 08/26/1977SE
K771398Shell VeneerELM · Traditional 08/26/1977SE
K771403Ease (Modification to)EJJ · Traditional 08/22/1977SE

Questions and answers

When was Composite Restorative cleared by the FDA?

Composite Restorative (K802262) received a 510(k) decision of Unknown on September 16, 1980, 0 days after the submission was received.