← FDA Medical Device Classifications
Laparoscopic Bladder-Neck Suspension Instrument, Stress Urinary Incontinence
OCQ · Class II — Moderate Risk (510(k) clearance required) · Obstetrics/Gynecology · 21 CFR 884.1720
Classification
- FDA Product Code
OCQ- Device class
- Class II — Moderate Risk (510(k) clearance required)
- Regulation
- 21 CFR 884.1720
- Review panel
- GU
- Medical specialty
- Obstetrics/Gynecology
- Submission type
- 1
- GMP exempt
- N
- Life sustaining
- N
- Implant
- N
- Third-party review
- Y
Definition
For female urinary stress incontinence due to hypermobility
Market data
- Cleared 510(k) submissions
- 0
- Registered establishments
- 0
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown