510(k) K830276
K830276 is an FDA 510(k) premarket notification submitted by Ritmed, Inc. for the device "SECURET DRAPE & INSTRUMENT RETAINER/INCL". The FDA issued a decision of Substantially Equivalent on March 29, 1983. The device falls under product code GTC (Antisera, All Types, Klebsiella Spp.), a Class I device regulated under 21 CFR 866.3340. Ritmed, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 29, 1983
- Date Received
- January 25, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Antisera, All Types, Klebsiella Spp.
- Device Class
- Class I
- Regulation Number
- 866.3340
- Review Panel
- MI
- Submission Type