CardioCurve Steerable Sheath Small Curl, 40cm (CC-1040S ); CardioCurve Steerable Sheath Medium Curl, 40cm (CC-1040M ); CardioCurve Steerable Sheath Large Curl, 40cm (CC-1040L ); CardioCurve Steerable Sheath Small Curl, 61cm (CC-1061S); CardioCurve Steerable Sheath Medium Curl, 61cm (CC-1061M ); CardioCurve Steerable Sheath Large Curl, 61cm (CC-1061L); CardioCurve Steerable Sheath Small Curl, 71cm (CC-1071S ); CardioCurve Steerable Sheath Medium Curl, 71cm (CC-1071M ); CardioCurve Steer
K240004 is the FDA 510(k) clearance record for CardioCurve Steerable Sheath Small Curl, 40cm (CC-1040S ); CardioCurve Steerable Sheath Medium Curl, 40cm (CC-1040M ); CardioCurve Steerable Sheath Large Curl, 40cm (CC-1040L ); CardioCurve Steerable Sheath Small Curl, 61cm (CC-1061S); CardioCurve Steerable Sheath Medium Curl, 61cm (CC-1061M ); CardioCurve Steerable Sheath Large Curl, 61cm (CC-1061L); CardioCurve Steerable Sheath Small Curl, 71cm (CC-1071S ); CardioCurve Steerable Sheath Medium Curl, 71cm (CC-1071M ); CardioCurve Steer, a class II device, cleared for Circa Scientific, Inc. on under FDA product code DYB (Introducer, Catheter). FDA records list 8 510(k) clearances for Circa Scientific, Inc., from to . As of , FDA records show no recalls naming K240004.
Clearance record
- Decision date
- Received
- (29 days to decision)
- Product code
- DYB Introducer, Catheter
- Regulation
- 21 CFR 870.1340
- Device class
- Class II
- Review panel
- Cardiovascular
- Applicant
- Circa Scientific, Inc. 14 Inverness Dr. E, Suite H-136, Englewood CO
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code DYB
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 2 |
| January 2026 | 1 |
| February 2026 | 2 |
| March 2026 | 1 |
| April 2026 | 7 |
| May 2026 | 0 |
| June 2026 | 3 |
| July 2026 | 2 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
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