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

Laparoscopic Contraceptive Tubal Occlusion Device

21 CFR 884.5380 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

KNH is the FDA product code for Laparoscopic Contraceptive Tubal Occlusion Device, a class III device type, regulated under 21 CFR 884.5380. FDA's definition for this code reads: "Call for PMAs to be filed by 12/30/87 (52 FR 36883 (10/1/87))". As of , FDA records hold no 510(k) clearances under this code and 4 recalls.

Classification record

Product code
KNH
Device name
Laparoscopic Contraceptive Tubal Occlusion Device
FDA definition
Call for PMAs to be filed by 12/30/87 (52 FR 36883 (10/1/87))
Regulation
21 CFR 884.5380
Device class
Class III
Review panel
Obstetrics/Gynecology
Submission type
PMA
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
4

Companies listing this code with FDA

Companies whose registered establishments list this code