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

Applicator (Laryngo-Tracheal), Topical Anesthesia

21 CFR 868.5170 / Anesthesiology
FDA source (opens on fda.gov)

CCT is the FDA product code for Applicator (Laryngo-Tracheal), Topical Anesthesia, a class II device type, regulated under 21 CFR 868.5170. As of , FDA records hold 10 510(k) clearances under this code, the most recent dated , and 6 recalls.

Classification record

Product code
CCT
Device name
Applicator (Laryngo-Tracheal), Topical Anesthesia
Regulation
21 CFR 868.5170
Device class
Class II
Review panel
Anesthesiology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
10
Ingested recalls
6

Clearances, product code CCT

By decision year
10 clearances under product code CCT with a decision year between 1976 and 2024, 1976 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code CCT by decision year
YearClearances
19762
19811
19901
20001
20071
20111
20161
20181
20241

Applicants with the most clearances

Product code CCT
Applicants holding the most 510(k) clearances under product code CCT
ApplicantClearances
Sherwood Medical Industries2
Ackrad Laboratories1
Astra Pharmaceutical Products, Inc.1
Dualams, Inc., dba Airkor1
Medica Holdings, LLC1
N.M. Beale Co., Inc.1
Sharn, Inc.1
Teleflex Medical1
Wolfe Tory Medical, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code