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FDA 510(k)

ASPRI-LUKE

K-Number: K791847 · 1979-10-02

ApplicantMedical Marketing Group
Decision Date1979-10-02
Product CodeBYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ASPRI-LUKE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Marketing Group. It received FDA 510(k) clearance on 1979-10-02 under 510(k) number K791847. 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 ASPRI-LUKE?

ASPRI-LUKE is a medical device that received FDA 510(k) clearance on 1979-10-02. The listed applicant is Medical Marketing Group. The 510(k) number is K791847.

When did ASPRI-LUKE receive FDA 510(k) clearance?

ASPRI-LUKE received FDA 510(k) clearance on 1979-10-02, under 510(k) number K791847.

Who is the listed applicant for ASPRI-LUKE?

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

What is the FDA product code for ASPRI-LUKE?

The FDA product code for ASPRI-LUKE is BYZ.

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Other records listing Medical Marketing Group 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.

K910022MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KITK884819O'NEIL URINARY CATHETER INTRODUCERK874682MMG CATHETER PLUG W/DRAINAGE TUBE COVERK871999MMG URO-SELF CATHETERK863912THE MMG 5 IN 1 CONNECTORK840838MMG CONNECTIVE TUBING

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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 IndustriesK834467SPECIMEN TRAPMicrovasive

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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