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FDA 510(k)

ARGYLE ASPIR-FLEX SUCTION CATHETER

K-Number: K925556 · 1993-07-30

ApplicantSherwood Medical Co.
Decision Date1993-07-30
Product CodeBSY
Advisory CommitteeAN
DecisionUnknown

Device Summary

ARGYLE ASPIR-FLEX SUCTION CATHETER 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 1993-07-30 under 510(k) number K925556. The device is classified under product code BSY. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the ARGYLE ASPIR-FLEX SUCTION CATHETER?

ARGYLE ASPIR-FLEX SUCTION CATHETER is a medical device that received FDA 510(k) clearance on 1993-07-30. The listed applicant is Sherwood Medical Co.. The 510(k) number is K925556.

When did ARGYLE ASPIR-FLEX SUCTION CATHETER receive FDA 510(k) clearance?

ARGYLE ASPIR-FLEX SUCTION CATHETER received FDA 510(k) clearance on 1993-07-30, under 510(k) number K925556.

Who is the listed applicant for ARGYLE ASPIR-FLEX SUCTION CATHETER?

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 ARGYLE ASPIR-FLEX SUCTION CATHETER?

The FDA product code for ARGYLE ASPIR-FLEX SUCTION CATHETER is BSY.

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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: BSY)

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.

K031997MALLINCKRODT DAR TY-CARE / TY-CARE EXEL CLOSED SUCTION SYSTEMMallinckrodt Dar S.R.L.K992902AMBU HAND POWER SUCTION PUMPAmbu, Inc.K982945DUAL PURPOSE CLOSED CATHETERSpirit Medical Systems, Inc.K981910SUCTION CATHETERNi-Med, Inc.K972258HI-CARE CLOSED SUCTION SYSTEMMallinckrodt MedicalK973199AMSINO SUCTION CATHETERAmsino Intl., Inc.

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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