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FDA 510(k)

BIOPSY FORCEPS, (NON-RIGID)

K-Number: K896146 · 1990-03-09

ApplicantPortlyn Corp.
Decision Date1990-03-09
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

BIOPSY FORCEPS, (NON-RIGID) is the device name listed in this FDA 510(k) record. The listed applicant is Portlyn Corp.. It received FDA 510(k) clearance on 1990-03-09 under 510(k) number K896146. 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 BIOPSY FORCEPS, (NON-RIGID)?

BIOPSY FORCEPS, (NON-RIGID) is a medical device that received FDA 510(k) clearance on 1990-03-09. The listed applicant is Portlyn Corp.. The 510(k) number is K896146.

When did BIOPSY FORCEPS, (NON-RIGID) receive FDA 510(k) clearance?

BIOPSY FORCEPS, (NON-RIGID) received FDA 510(k) clearance on 1990-03-09, under 510(k) number K896146.

Who is the listed applicant for BIOPSY FORCEPS, (NON-RIGID)?

The FDA 510(k) record lists Portlyn Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIOPSY FORCEPS, (NON-RIGID)?

The FDA product code for BIOPSY FORCEPS, (NON-RIGID) is EOQ.

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Other records listing Portlyn Corp. 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.

K970083DYNABITE HOT GI BIOPSY FORCEPSK951447DYNABITE CARDIOVASCULAR BIOPSY FORCEPSK952391DYNABITE UROLOGICAL FORCEPSK944245DYNABITE LAPAROSCOPIC FORCEPSK934506DYNABITE HYSTEROSCOPIC FORCEPSK901300BIOPSY FORCEPS

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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

View on FDA Database →

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

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