Cleared Traditional

K962743 - PULPDENT SODIUM HYPOCHLORITE SOLUTION
(FDA 510(k) Clearance)

K962743 · Pulpdent Corp. · Dental

Aug 1996

Decision

22d

Days

—

Risk

K962743 is an FDA 510(k) clearance for the PULPDENT SODIUM HYPOCHLORITE SOLUTION. This device is classified as a Cleanser, Root Canal.

Submitted by Pulpdent Corp. (Watertown, US). The FDA issued a Cleared decision on August 6, 1996, 22 days after receiving the submission on July 15, 1996.

This device falls under the Dental FDA review panel.

Submission Details

510(k) Number	K962743 FDA.gov
FDA Decision	Cleared SESE
Date Received	July 15, 1996
Decision Date	August 06, 1996
Days to Decision	22 days
Submission Type	Traditional
Review Panel	Dental (DE)
Summary	Summary PDF