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FDA 510(k)

OHMEDA ADAPTABLE CABLE W/DETACHABLE SENSOR

K-Number: K930081 · 1993-11-04

ApplicantOhmeda Monitoring Systems
Decision Date1993-11-04
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

OHMEDA ADAPTABLE CABLE W/DETACHABLE SENSOR is the device name listed in this FDA 510(k) record. The listed applicant is Ohmeda Monitoring Systems. It received FDA 510(k) clearance on 1993-11-04 under 510(k) number K930081. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OHMEDA ADAPTABLE CABLE W/DETACHABLE SENSOR?

OHMEDA ADAPTABLE CABLE W/DETACHABLE SENSOR is a medical device that received FDA 510(k) clearance on 1993-11-04. The listed applicant is Ohmeda Monitoring Systems. The 510(k) number is K930081.

When did OHMEDA ADAPTABLE CABLE W/DETACHABLE SENSOR receive FDA 510(k) clearance?

OHMEDA ADAPTABLE CABLE W/DETACHABLE SENSOR received FDA 510(k) clearance on 1993-11-04, under 510(k) number K930081.

Who is the listed applicant for OHMEDA ADAPTABLE CABLE W/DETACHABLE SENSOR?

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

What is the FDA product code for OHMEDA ADAPTABLE CABLE W/DETACHABLE SENSOR?

The FDA product code for OHMEDA ADAPTABLE CABLE W/DETACHABLE SENSOR is DQO.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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