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FDA 510(k)

ARGLE LATEX PENROSE TUBING

K-Number: K802286 · 1980-10-23

ApplicantSherwood Medical Co.
Decision Date1980-10-23
Product CodeKGZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ARGLE LATEX PENROSE TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1980-10-23 under 510(k) number K802286. The device is classified under product code KGZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGLE LATEX PENROSE TUBING?

ARGLE LATEX PENROSE TUBING is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is Sherwood Medical Co.. The 510(k) number is K802286.

When did ARGLE LATEX PENROSE TUBING receive FDA 510(k) clearance?

ARGLE LATEX PENROSE TUBING received FDA 510(k) clearance on 1980-10-23, under 510(k) number K802286.

Who is the listed applicant for ARGLE LATEX PENROSE TUBING?

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

What is the FDA product code for ARGLE LATEX PENROSE TUBING?

The FDA product code for ARGLE LATEX PENROSE TUBING is KGZ.

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Other records listing Sherwood Medical Co. 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.

K981365MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONSK960982MONOJECT BLUNT I.V. ACCESS CANNULA/MONOJECT HYPODERMIC SYRINGE WITH BLUNT I.V. ACCESS CANNULAK962880SENSI-TOUCH COMBO SPINAL/EPIDURAL REGIONAL ANESTHESIA DELIVERY SYSTEMK960574ARGYLE TURKEL NEONATAL/PEDIATRIC THORACIC CATHETER INSERTION TRAY AND THORACIC CATHETER SYSTEMK960677KANGAROO JEJUNAL FEEDING SYSTEMK960632KANGAROO FEEDING TUBE PLACMENT STYLET

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Related Devices (Code: KGZ)

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.

K022306AART SILICONE TUBINGAesthetic and Reconstructive Technologies, Inc.K974295BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBINGByron MedicalK973183WOUND DRAINAGE HOLDERR & D Medical Products, Inc.K955433DURALASTIC SILICONE TUBINGAllied Biomedical Corp.K942315NAVARRE PERCUTANEOUS ACCESS SETNavarre Biomedical , Ltd.K896087PALESTRANT IRRIGATION AND DRAINAGE SETNorth American Instrument Corp.

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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