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FDA 510(k)

PILLING WECK SURGICAL Y STENT FORCEPS

K-Number: K990547 · 1999-04-27

ApplicantPilling Weck, Inc.
Decision Date1999-04-27
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PILLING WECK SURGICAL Y STENT FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Weck, Inc.. It received FDA 510(k) clearance on 1999-04-27 under 510(k) number K990547. 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 PILLING WECK SURGICAL Y STENT FORCEPS?

PILLING WECK SURGICAL Y STENT FORCEPS is a medical device that received FDA 510(k) clearance on 1999-04-27. The listed applicant is Pilling Weck, Inc.. The 510(k) number is K990547.

When did PILLING WECK SURGICAL Y STENT FORCEPS receive FDA 510(k) clearance?

PILLING WECK SURGICAL Y STENT FORCEPS received FDA 510(k) clearance on 1999-04-27, under 510(k) number K990547.

Who is the listed applicant for PILLING WECK SURGICAL Y STENT FORCEPS?

The FDA 510(k) record lists Pilling Weck, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PILLING WECK SURGICAL Y STENT FORCEPS?

The FDA product code for PILLING WECK SURGICAL Y STENT FORCEPS is EOQ.

Related Clinical Trials

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.

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Other records listing Pilling Weck, 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.

K974250VERSASTAT MULTIPOLAR SCISSORS AND CABLESK962771BURKE CONGENITAL THORACOSCOPY INSTRUMENTSK945520HEMOCLIP ECOSYSTEMK944552PILLING WECK M-20 DISPOSABLE AUTOMATIC HEMOCLIPK943719VISISTAT STAPLER

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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