Atlas FDA

BXJ

4 FDA 510(k) clearances · Product code

FDA profile

Official device name
Clip, Nose
Device class
Class I (low risk)
Regulation
21 CFR 868.6225
Medical specialty
Anesthesiology
Flags
GMP exempt
Adverse events (MAUDE)
2000: 1
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
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RecordFirmDate
MEDIPART DISPOS. NOSE CLIP MP-2001 (K853578)Medipart Jerry Alexander1985-10-29
NOSECLIP #6118 (K810339)Todd Industries, Inc.1981-03-17
NOSECLIP FOR RESP. CARE & PULMON. FUNC. (K770015)Bd Becton Dickinson Vacutainer Systems Preanalytic1977-03-16
NOSE CLIP (K760461)Inspiron Corp.1976-08-26

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Every clearance here is in the API, with alerts when new ones post.