Isolator® Linear Pen (MLP1); Isolator® Transpolar™ Pen (MAX1, MAX5), Coolrail® Linear Pen (MCR1); Isolator® Synergy Surgical Ablation System (EMR2, EML2); Isolator® Synergy™ EnCompass Clamp (OLH, OSH) and Guide System; Isolator® Synergy Access Clamp (EMT1)
K221358 is the FDA 510(k) clearance record for Isolator® Linear Pen (MLP1); Isolator® Transpolar™ Pen (MAX1, MAX5), Coolrail® Linear Pen (MCR1); Isolator® Synergy Surgical Ablation System (EMR2, EML2); Isolator® Synergy™ EnCompass Clamp (OLH, OSH) and Guide System; Isolator® Synergy Access Clamp (EMT1), a class II device, cleared for AtriCure, Inc. on under FDA product code OCL (Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue). FDA's definition for product code OCL reads: "Surgical device for cutting, coagulation, and/or ablation of tissue, including cardiac tissue". FDA records list 59 510(k) clearances for AtriCure, Inc., from to . As of , FDA records show no recalls naming K221358.
Clearance record
- Decision date
- Received
- (233 days to decision)
- Product code
- OCL Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue
- Regulation
- 21 CFR 878.4400
- Device class
- Class II
- Review panel
- General, Plastic Surgery
- Applicant
- AtriCure, Inc. 7555 Innovation Way, Mason OH
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code OCL
Trailing 12 monthsFDA records hold no clearances under product code OCL in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
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