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FDA 510(k)

ARGYLE TURKEL SAFETY PNEUMOTHORAX PROCEDURE TRAY

K-Number: K934428 · 1993-12-30

ApplicantSherwood Medical Co.
Decision Date1993-12-30
Product CodeLRO
Advisory CommitteeSU
DecisionUnknown

Device Summary

ARGYLE TURKEL SAFETY PNEUMOTHORAX PROCEDURE TRAY 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 1993-12-30 under 510(k) number K934428. The device is classified under product code LRO. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the ARGYLE TURKEL SAFETY PNEUMOTHORAX PROCEDURE TRAY?

ARGYLE TURKEL SAFETY PNEUMOTHORAX PROCEDURE TRAY is a medical device that received FDA 510(k) clearance on 1993-12-30. The listed applicant is Sherwood Medical Co.. The 510(k) number is K934428.

When did ARGYLE TURKEL SAFETY PNEUMOTHORAX PROCEDURE TRAY receive FDA 510(k) clearance?

ARGYLE TURKEL SAFETY PNEUMOTHORAX PROCEDURE TRAY received FDA 510(k) clearance on 1993-12-30, under 510(k) number K934428.

Who is the listed applicant for ARGYLE TURKEL SAFETY PNEUMOTHORAX PROCEDURE TRAY?

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 TURKEL SAFETY PNEUMOTHORAX PROCEDURE TRAY?

The FDA product code for ARGYLE TURKEL SAFETY PNEUMOTHORAX PROCEDURE TRAY is LRO.

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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: LRO)

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.

K213481Medline General Surgery TrayMedline Industries, Inc.K212258Medline Cardiovascular Procedure KitMedline Industries, Inc.K041080SURGICAL DRAPE KIT - D.I.R.R.A. SRLD.I.R.R.A. S.R.L.K030721QUICK-TAP PARACENTESIS TRAY, KIT & NEEDLEBallard Medical ProductsK023276AMSINO TRACHEOSTOMY CARE TRAYAmsino International, Inc.K980137WORLDWIDE MEDICAL TECHNOLOGIES BONE MARROW BIOPSY PROCEDURE TRAYWorldwide Medical Technologies, LLC

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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