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

Chest Drainage Kit

21 CFR 880.6740 / General Hospital
FDA source (opens on fda.gov)

PAD is the FDA product code for Chest Drainage Kit, a class II device type, regulated under 21 CFR 880.6740. 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 20 recalls.

Classification record

Product code
PAD
Device name
Chest Drainage 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 880.6740
Device class
Class II
Review panel
General Hospital
Submission type
FDA code 7
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
0
Ingested recalls
20

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 20 companies shown, in name order