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FDA 510(k)

CARDIAC CATHETERIZATION TRAY

K-Number: K931560 · 1994-07-11

ApplicantClinipad Corp.
Decision Date1994-07-11
Product CodeDQO
Advisory CommitteeCV
DecisionUnknown

Device Summary

CARDIAC CATHETERIZATION TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Clinipad Corp.. It received FDA 510(k) clearance on 1994-07-11 under 510(k) number K931560. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CARDIAC CATHETERIZATION TRAY?

CARDIAC CATHETERIZATION TRAY is a medical device that received FDA 510(k) clearance on 1994-07-11. The listed applicant is Clinipad Corp.. The 510(k) number is K931560.

When did CARDIAC CATHETERIZATION TRAY receive FDA 510(k) clearance?

CARDIAC CATHETERIZATION TRAY received FDA 510(k) clearance on 1994-07-11, under 510(k) number K931560.

Who is the listed applicant for CARDIAC CATHETERIZATION TRAY?

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

What is the FDA product code for CARDIAC CATHETERIZATION TRAY?

The FDA product code for CARDIAC CATHETERIZATION TRAY is DQO.

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Other records listing Clinipad Corp. 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.

K931668PICC INSERTION TRAYK932071I.V. START KITK932010V.A.D. ACCESS KITK932036LACERATION TRAYK932016TRACHEOSTOMY CARE TRAYK862562PUNCH BIOPSY KIT

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Related Devices (Code: DQO)

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.

K261455Arterial Pressure Monitoring Set/TraySpectrum VascularK252702Bioptimal Pulmonary Artery Monitoring Catheter (TD2502NF, TD2502NGF, TD2502NDF, TD2502NCF, TD2502NCGF, TD2502NDGF, TD2502NDCF, TD2502NDCGF, TD2502NXCF, TD2502NDXF, TD2502NXCGF, TD2502NDXGF, TD2502NDXCF, TD2502NDXCGF, TD2502-110NF, TD2502-110NGF, TD2502-110NDF, TD2502-110NCF, TD2502-110NDGF, TD2502-110NDCF, TD2502-110NCGF, TD2502-110NDCGF, TD2502-110NXF, TD2502-110NXGF, TD2502-110NDXF, TD2502-110NXCF, TD2502-110NDXGF, TD2502-110NDXCF ,TD2502-110NXCGF, TD2502-110NDXCGF, TD2602NF, TD2602NBioptimal International Pte. , Ltd.K254278Arterial Pressure Monitoring Set/TraySpectrum VascularK250751DualView CatheterTerumo CorporationK242966Gentuity® HF-OCT Imaging System with Vis-Rx Prime® Micro-Imaging CatheterGentuity, LLCK242420pNOVUS 21 MicrocatheterPhenox, Ltd.

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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