← FDA Medical Device Classifications

Pump, Air, Non-Manual, For Endoscope

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

Classification

FDA Product Code

FEQ

Device class

Class II — Moderate Risk (510(k) clearance required)

Regulation

21 CFR 876.1500

Review panel

GU

Medical specialty

Gastroenterology, Urology

Submission type

1

GMP exempt

N

Life sustaining

N

Implant

N

Third-party review

N

Market data

Cleared 510(k) submissions

21

Registered establishments

46

Source

Authoritative

FDA Device Classification database

Machine

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