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

Epidural Anesthesia Kit

21 CFR 868.5120 / Anesthesiology
FDA source (opens on fda.gov)

OGE is the FDA product code for Epidural Anesthesia Kit, a class II device type, regulated under 21 CFR 868.5120. 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 33 recalls.

Classification record

Product code
OGE
Device name
Epidural Anesthesia 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 868.5120
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
33

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 25 companies shown, in name order