Cleared Traditional

K863670 - VISION (TM) CALCIUM (FDA 510(k) Clearance)

Nov 1986
Decision
56d
Days
Class 2
Risk

K863670 is an FDA 510(k) clearance for the VISION (TM) CALCIUM. This device is classified as a Cresolphthalein Complexone, Calcium (Class II - Special Controls, product code CIC).

Submitted by Abbott Laboratories (Abbott Park, US). The FDA issued a Cleared decision on November 13, 1986, 56 days after receiving the submission on September 18, 1986.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1145.

Submission Details

510(k) Number K863670 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 18, 1986
Decision Date November 13, 1986
Days to Decision 56 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary

Device Classification

Product Code CIC — Cresolphthalein Complexone, Calcium
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.1145