510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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KTZClass I

Caliper

21 CFR 888.4150 / Orthopedic
FDA source (opens on fda.gov)

KTZ is the FDA product code for Caliper, a class I device type, regulated under 21 CFR 888.4150. As of , FDA records hold 7 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
KTZ
Device name
Caliper
Regulation
21 CFR 888.4150
Device class
Class I
Review panel
Orthopedic
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
7
Ingested recalls
0

Clearances, product code KTZ

By decision year
7 clearances under product code KTZ with a decision year between 1976 and 1992, 1976 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KTZ by decision year
YearClearances
19761
19801
19811
19821
19831
19841
19921

Applicants with the most clearances

Product code KTZ
Applicants holding the most 510(k) clearances under product code KTZ
ApplicantClearances
Caldwell, Justiss & Co., Inc.1
Dr. Micheal A. Sabia1
Fitness Motivation Institute of America1
Mcgaw Laboratories1
Nk Biotechnical Engineering Co.1
Twin City Surgical, Inc.1
Warner-Lambert Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 177 companies shown, in name order