← FDA Medical Device Classifications

Endoscope Introducer Kit

NWU · Class II — Moderate Risk (510(k) clearance required) · Gastroenterology, Urology · 21 CFR 876.1500

Classification

FDA Product Code
NWU
Device class
Class II — Moderate Risk (510(k) clearance required)
Regulation
21 CFR 876.1500
Review panel
GU
Medical specialty
Gastroenterology, Urology
Submission type
7
GMP exempt
N
Life sustaining
N
Implant
N
Third-party review
N

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.

Market data

Cleared 510(k) submissions
3
Registered establishments
36

Source

Authoritative
FDA Device Classification database
Machine
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