510(k) K853583
K853583 is an FDA 510(k) premarket notification submitted by Modern Medical Products for the device "MODERN MEDICAL PRODUCTS TOWEL CLAMP". The FDA issued a decision of Substantially Equivalent on Sep 16, 1985. The device falls under product code GDJ (Clamp, Surgical, General & Plastic Surgery), a Class I device regulated under 21 CFR 878.4800.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Sep 16, 1985
- Date Received
- Aug 26, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Clamp, Surgical, General & Plastic Surgery
- Device Class
- Class I
- Regulation Number
- 878.4800
- Review Panel
- SU
- Submission Type
- 510(k) Exempt