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

Orotracheal Intubation Guide Kit

21 CFR 868.1400 / Anesthesiology
FDA source (opens on fda.gov)

OGK is the FDA product code for Orotracheal Intubation Guide Kit, a class II device type, regulated under 21 CFR 868.1400. FDA's definition for this code reads: "This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. This kit, as described in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k))...". As of , FDA records hold no 510(k) clearances under this code and 2 recalls.

Classification record

Product code
OGK
Device name
Orotracheal Intubation Guide Kit
FDA definition
This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. This kit, as described in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market.
Regulation
21 CFR 868.1400
Device class
Class II
Review panel
Anesthesiology
Submission type
FDA code 7
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
2

Companies listing this code with FDA

Companies whose registered establishments list this code