Insighters™ Single-use Bronchoscope/Insight Bimodel-Integral iS-B12A 4.6/2.0; Insighters™ Single-use Bronchoscope/Insight Bimodel-Integral iS-B22A 5.5 /2.6; Insighters™ Single-use Bronchoscope/Insight Bimodel-Integral iS-B26A 6.0/3.0; Insighters™ Insight Workstation iS-PF1.
K242793 is the FDA 510(k) clearance record for Insighters™ Single-use Bronchoscope/Insight Bimodel-Integral iS-B12A 4.6/2.0; Insighters™ Single-use Bronchoscope/Insight Bimodel-Integral iS-B22A 5.5 /2.6; Insighters™ Single-use Bronchoscope/Insight Bimodel-Integral iS-B26A 6.0/3.0; Insighters™ Insight Workstation iS-PF1., a class II device, cleared for Shenzhen Insighters Medical Technology Co., Ltd. on under FDA product code EOQ (Bronchoscope (Flexible Or Rigid)). FDA's definition for product code EOQ reads: "A bronchoscope (flexible or rigid) and accessories is a tubular endoscopic device with any of a group of accessory devices which attach to the bronchoscope and is intended to examine or treat the larynx and tracheobronchial tree. If the...". FDA records list 3 510(k) clearances for Shenzhen Insighters Medical Technology Co., Ltd., from to . As of , FDA records show no recalls naming K242793.
Clearance record
- Decision date
- Received
- (254 days to decision)
- Product code
- EOQ Bronchoscope (Flexible Or Rigid)
- Regulation
- 21 CFR 874.4680
- Device class
- Class II
- Review panel
- Ear, Nose, Throat
- Applicant
- Shenzhen Insighters Medical Technology Co., Ltd. The 13th Floor Of Hengtemei Bldg., Ganli Rd. #3, Shenzhen, CN
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code EOQ
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 2 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 2 |
| May 2026 | 1 |
| June 2026 | 1 |
| July 2026 | 2 |
| August 2026 | 0 |
| September 2026 | 3 |
| October 2026 | 0 |
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