3M LITTMANN
FDA 510(k) clearance K003723 · decided 2001-03-27
Clearance details
- K-number
- K003723
- Device name
- 3M LITTMANN
- Applicant
- 3M Company
- Decision
- Substantially Equivalent
- Date received
- 2000-12-04
- Decision date
- 2001-03-27
- Days to decision
- 113 days
- Clearance type
- Abbreviated
- Product code
- DQD
- Device class
- 2
- Regulation number
- 870.1875
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- St. Paul, MN, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch 3M Company
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| Smart Wireless Stethoscope (STEMO310);Smart Wireless Stethoscope (STEMO710);Smart Wireless Stethoscope (STEMO720);Smart Wireless Stethoscope (STEMO730) (K261494) | Shanghai Hulu Devices Co., Ltd. | 2026-07-31 |
| CORE 300 Digital Stethoscope (K261694) | Eko Health, Inc. | 2026-07-23 |
| AiSteth® (K252915) | Ai Health Highway India Pvt., Ltd. | 2026-05-22 |
| Tyto Stethoscope (G3) (K252089) | Tyto Care , Ltd. | 2026-03-12 |
| Kneevoice Cartilage Evaluation System (750-3600-001) (K252076) | Kneevoice, Inc. | 2026-02-06 |
| eMurmur Heart AI (K252284) | Csd Labs | 2025-12-19 |
| Stethophone Pro (K252595) | Sparrow Acoustics, Inc. | 2025-09-12 |
| Eko Foundation Analysis Software with Transformers (EFAST) (K251494) | Eko Health, Inc. | 2025-08-12 |
| AccurSound Electronic Stethoscope (AS101) (K242971) | Heroic Faith International , Ltd. | 2024-11-25 |
| Stethophone (K240901) | Sparrow Acoustics, Inc. | 2024-09-19 |
| Keikku Electronic stethoscope (K233313) | Lapsi Health Holding B.V. | 2024-04-10 |
| CORE 500 Digital Stethoscope (K233609) | Eko Health, Inc. | 2024-03-28 |
Recalls involving this device
No recalls on record reference this clearance.
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S011) | 3M Company | 1994-11-28 |
| CENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S010) | 3M Company | 1994-05-19 |
| KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S006) | 3M Company | 1992-12-31 |
| KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S009) | 3M Company | 1992-03-13 |
| KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S008) | 3M Company | 1992-01-28 |
| KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S007) | 3M Company | 1990-10-17 |
| KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S005) | 3M Company | 1990-03-08 |
| KENNEDY LAD(TM) LIGAMENT AUGMENTATION DEVICE (P850069/S004) | 3M Company | 1989-11-22 |