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FDA 510(k)

TISSUE/POLYP TRAP SYSTEM

K-Number: K902883 · 1990-09-12

ApplicantTriton Technology, Inc.
Decision Date1990-09-12
Product CodeBYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TISSUE/POLYP TRAP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Triton Technology, Inc.. It received FDA 510(k) clearance on 1990-09-12 under 510(k) number K902883. The device is classified under product code BYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TISSUE/POLYP TRAP SYSTEM?

TISSUE/POLYP TRAP SYSTEM is a medical device that received FDA 510(k) clearance on 1990-09-12. The listed applicant is Triton Technology, Inc.. The 510(k) number is K902883.

When did TISSUE/POLYP TRAP SYSTEM receive FDA 510(k) clearance?

TISSUE/POLYP TRAP SYSTEM received FDA 510(k) clearance on 1990-09-12, under 510(k) number K902883.

Who is the listed applicant for TISSUE/POLYP TRAP SYSTEM?

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

What is the FDA product code for TISSUE/POLYP TRAP SYSTEM?

The FDA product code for TISSUE/POLYP TRAP SYSTEM is BYZ.

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Other records listing Triton Technology, 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.

K932142SUCTION GUILLOTINE DEVICEK911448MULTIPLE BIOPSY DEVICE-MBXK881303TRITON MODEL 100 PULSED DOPPLER BLOOD FLOWMETER

Related Devices (Code: BYZ)

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.

K925412ELECTROMEDICS TISSUE TRAP/ #TT280Electromedics, Inc.K913643MUCOUS SPECIMEN TRAPMedical Device Inspection Co., Inc.K841409BUSH NECK W/PLUGWarne Surgical Products, Ltd.K840253ONE-WAY AIR VALVEDelta Medical IndustriesK834467SPECIMEN TRAPMicrovasiveK822557SPECIMEN ADAPTORBemis Health Care

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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