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FDA 510(k)

CZAJA-MCCAFFREY RIGID STENT INTRODUCER/ENDOSCOPE

K-Number: K983878 · 1999-01-29

ApplicantE. Benson Hood Laboratories, Inc.
Decision Date1999-01-29
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

CZAJA-MCCAFFREY RIGID STENT INTRODUCER/ENDOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is E. Benson Hood Laboratories, Inc.. It received FDA 510(k) clearance on 1999-01-29 under 510(k) number K983878. The device is classified under product code EOQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CZAJA-MCCAFFREY RIGID STENT INTRODUCER/ENDOSCOPE?

CZAJA-MCCAFFREY RIGID STENT INTRODUCER/ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1999-01-29. The listed applicant is E. Benson Hood Laboratories, Inc.. The 510(k) number is K983878.

When did CZAJA-MCCAFFREY RIGID STENT INTRODUCER/ENDOSCOPE receive FDA 510(k) clearance?

CZAJA-MCCAFFREY RIGID STENT INTRODUCER/ENDOSCOPE received FDA 510(k) clearance on 1999-01-29, under 510(k) number K983878.

Who is the listed applicant for CZAJA-MCCAFFREY RIGID STENT INTRODUCER/ENDOSCOPE?

The FDA 510(k) record lists E. Benson Hood Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CZAJA-MCCAFFREY RIGID STENT INTRODUCER/ENDOSCOPE?

The FDA product code for CZAJA-MCCAFFREY RIGID STENT INTRODUCER/ENDOSCOPE is EOQ.

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Other records listing E. Benson Hood Laboratories, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K841350SALIVARY BYPASS TUBEK841349ESOPHAGEAL TUBEK841266MONTGOMERY TRACHEAL T-TUBEK841348UMBRELLA KEELK841347LARYNGEAL STENT

Related Devices (Code: EOQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261637Single-use Flexible BronchoscopeHunan Vathin Medical Instrument Co., Ltd.K260309Ambu® aScope™ 5 Broncho 2.7/1.2; Ambu® aScope™ 5 Broncho 4.2/2.2; Ambu® aScope™ 5 Broncho 4.2/2.2 Sampler SetAmbu A/SK2540263.8mm Slim ProVu Video Bronchoscope (090-02-0038U); 5.0mm Regular ProVu Video Bronchoscope (090-02-0050U); 6.0mm Large ProVu Video Bronchoscope (090-02-0060U); ProVu Video Bronchoscope 8 display (040-07-0082U)Flexicare Medical Limited.K260382MONARCH™ Platform (MON-000008)Auris Health, Inc.K254037LungFlow Airway CatheterFree Flow Medical, Inc.K253137FUJIFILM Endoscope Model EB-840S; FUJIFILM Endoscope Model EB-840TFujifilm Corporation

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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