CPR Heart Pack
FDA 510(k) K960209 · Custom Pack Reliability
510(k) numberK960209
Submission
- Device name
- CPR Heart Pack
- Applicant
- Custom Pack Reliability
Orlando, FL, US - Received
- January 16, 1996
- Decision date
- April 4, 1996
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- GAW – Suture, Nonabsorbable, Synthetic, Polypropylene
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.5010
- Specialty
- General, Plastic Surgery
- Implant
- Yes
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|---|---|---|---|
| K253572 | STRATAFIX Spiral PRONOVA Unidirectional Knotless Tissue Control Device STRATAFIX…GAW · Traditional | ETHICON, Inc. | 03/27/2026SE |
| K233355 | Cypris eXact Suturing SystemGAW · Traditional | Cypris Medical | 01/12/2024SE |
| K230746 | Non absorbable Surgical Polypropylene SutureGAW · Traditional | Shandong Haidike Medical Products Co., Ltd. | 09/14/2023SE |
| K221280 | VessealGAW · Traditional | Lydus Medical , Ltd. | 12/09/2022SE |
| K211178 | DURAMESH Mesh SutureGAW · Traditional | Msi | 09/02/2022SE |
| K192953 | APTOS Threads Polypropylene Surgical SuturesGAW · Traditional | Aptos, LLC | 08/27/2020SE |
| K193530 | Deklene MAXXGAW · Special | Teleflex Medical | 03/19/2020SE |
| K191299 | Silhouette Featherlift / Silhouette LiftGAW · Special | Silhouette Lift, Inc. | 06/14/2019SE |
| K173747 | RexleneGAW · Traditional | Sm Eng Co., Ltd. | 12/21/2018SE |
| K180321 | Aesculap Optilene Nonabsorbable SutureGAW · Special | Aesculap, Inc. | 03/07/2018SE |
More from Aesculap, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K960205 | CPR Tracheotomy Care TrayBTO · Traditional | 08/27/1996SE |
| K960243 | CPR C-Section Delivery PackMLS · Traditional | 05/23/1996SE |
| K960239 | CPR D & C TrayHHK · Traditional | 05/23/1996SE |
| K960216 | CPR Suction Catheter KitJOL · Traditional | 04/15/1996SE |
| K960213 | CPR Total Hip PackFRG · Traditional | 04/12/1996SE |
| K960211 | CPR Total Knee PackFRG · Traditional | 04/12/1996SE |
| K960210 | CPR Ortho Hand PackFRG · Traditional | 04/12/1996SE |
| K960206 | CPR Dressing Change TrayFRG · Traditional | 04/12/1996SE |
| K960215 | CPR Urethral Catheter TrayFCM · Traditional | 04/01/1996SE |
| K960214 | CPR Foley Cahteter KitFCM · Traditional | 04/01/1996SE |
Questions and answers
When was CPR Heart Pack cleared by the FDA?
CPR Heart Pack (K960209) received a 510(k) decision of Substantially Equivalent on April 4, 1996, 79 days after the submission was received.
What is the product code of K960209?
The FDA product code is GAW – Suture, Nonabsorbable, Synthetic, Polypropylene, a Class II (moderate risk) device regulated under 21 CFR 878.5010.