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FDA 510(k)

FIBEROPTIC CATHETER

K-Number: K880661 · 1988-05-02

ApplicantOptimed Technologies, Inc.
Decision Date1988-05-02
Product CodeDQO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

FIBEROPTIC CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Optimed Technologies, Inc.. It received FDA 510(k) clearance on 1988-05-02 under 510(k) number K880661. 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 FIBEROPTIC CATHETER?

FIBEROPTIC CATHETER is a medical device that received FDA 510(k) clearance on 1988-05-02. The listed applicant is Optimed Technologies, Inc.. The 510(k) number is K880661.

When did FIBEROPTIC CATHETER receive FDA 510(k) clearance?

FIBEROPTIC CATHETER received FDA 510(k) clearance on 1988-05-02, under 510(k) number K880661.

Who is the listed applicant for FIBEROPTIC CATHETER?

The FDA 510(k) record lists Optimed Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FIBEROPTIC CATHETER?

The FDA product code for FIBEROPTIC CATHETER is DQO.

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Other records listing Optimed Technologies, Inc. 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.

K972520OPTIVIEWK955276BOOSTER LITE 4 MOTORIZED SCOOTERK955275BOOSTER TROPHY 5 MOTORIZED SCOOTERK955274BOOSTER LITE 3 MOTORIZED SCOOTERK943598FLEXIBLE FIBER OPTIC LAPAROSCOPESK926597LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES)

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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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