Lateral obturator BB2402-3

• FDA 510(k) K854414 decided 12 Mar 1986 Active
• FDA GUDID UDI-DI 03700620600730 listed 26 Oct 2023 Listed

1. 12 Mar 1986 Cleared FDA 510(k) K854414
2. 26 Oct 2023 Listed FDA GUDID 03700620600730

Trade name

Lateral obturator

Generic name

Rigid optical bronchoscope

Model / reference

BB2402-3

Primary DI / UDI-DI

03700620600730

510(k) Number

K854414 ↗

FDA product code

EOQ

GMDN term

Rigid optical bronchoscope

Device class

Class II

Regulation number

874.4680

GUDID distribution status

In Commercial Distribution

Sterilisation method

Moist Heat or Steam Sterilization

Category: Rigid optical bronchoscope

Other devices filed under FDA product code EOQ (Bronchoscope (Flexible Or Rigid)).

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• Rescue Pulmonary Grasping Forceps by Anrei Medical (Hangzhou) Co., Ltd.
• YIELD TISSUE SAMPLER by Broncus Technologies, Inc.
• GlideScope BFlex 5.8 Single-Use Bronchoscope by Verathon Medical (Canada) ULC
• Ion™ Endoluminal System (Ion™ Fully Articulating Catheter) (IF1000) by Intuitive Surgical, Inc.

• Adult introducer tube BR2000-3

  Class II

  FDA 510(k) K854414 Active Cleared 12 Mar 1986 GUDID on market

• Sterilization basket without lid DJ-4561

  Class II

  FDA 510(k) K854414 Active Cleared 12 Mar 1986 GUDID on market

• Pediatric tube BT2403-3

  Class II

  FDA 510(k) K854414 Active Cleared 12 Mar 1986 GUDID on market

• Pediatric plunger BP2402-3

  Class II

  FDA 510(k) K854414 Active Cleared 12 Mar 1986 GUDID on market

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