Cleared Traditional

TUMORIMETER

K874352 · Cancer Technologies, Inc. · General & Plastic Surgery

Nov 1987

Decision

31d

Days

Class 1

Risk

About This 510(k) Submission

K874352 is an FDA 510(k) clearance for the TUMORIMETER, a Tape, Measuring, Rulers And Calipers (Class I — General Controls, product code FTY), submitted by Cancer Technologies, Inc. (Tucson, US). The FDA issued a Cleared decision on November 23, 1987, 31 days after receiving the submission on October 23, 1987. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4800.

Submission Details

510(k) Number	K874352 FDA.gov
FDA Decision	Cleared SESE
Date Received	October 23, 1987
Decision Date	November 23, 1987
Days to Decision	31 days
Submission Type	Traditional
Review Panel	General & Plastic Surgery (SU)
Summary	—