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FDA 510(k)

SPECIMEN TRAP

K-Number: K834467 · 1984-02-17

ApplicantMicrovasive
Decision Date1984-02-17
Product CodeBYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SPECIMEN TRAP is the device name listed in this FDA 510(k) record. The listed applicant is Microvasive. It received FDA 510(k) clearance on 1984-02-17 under 510(k) number K834467. 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 SPECIMEN TRAP?

SPECIMEN TRAP is a medical device that received FDA 510(k) clearance on 1984-02-17. The listed applicant is Microvasive. The 510(k) number is K834467.

When did SPECIMEN TRAP receive FDA 510(k) clearance?

SPECIMEN TRAP received FDA 510(k) clearance on 1984-02-17, under 510(k) number K834467.

Who is the listed applicant for SPECIMEN TRAP?

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

What is the FDA product code for SPECIMEN TRAP?

The FDA product code for SPECIMEN TRAP is BYZ.

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Other records listing Microvasive 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.

K872771LOW PROFILE GASTROSTOMYK870705THERMAL COAGULATORK861323REPLACEMENT GASTROSTOMY TUBEK861309JEJUNAL FEEDING TUBEK860589INFLATOR/DEFLATOR PISTON SYRINGEK860366CHALLENGER HOT BIOPSY FORCEPS

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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.K902883TISSUE/POLYP TRAP SYSTEMTriton Technology, Inc.K841409BUSH NECK W/PLUGWarne Surgical Products, Ltd.K840253ONE-WAY AIR VALVEDelta Medical IndustriesK822557SPECIMEN 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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