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FDA 510(k)

LOPER CELIAC PLEXUS BLOCK CATHETER KIT

K-Number: K895955 · 1990-02-22

ApplicantOpticon Medical, Inc.
Decision Date1990-02-22
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LOPER CELIAC PLEXUS BLOCK CATHETER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Opticon Medical, Inc.. It received FDA 510(k) clearance on 1990-02-22 under 510(k) number K895955. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOPER CELIAC PLEXUS BLOCK CATHETER KIT?

LOPER CELIAC PLEXUS BLOCK CATHETER KIT is a medical device that received FDA 510(k) clearance on 1990-02-22. The listed applicant is Opticon Medical, Inc.. The 510(k) number is K895955.

When did LOPER CELIAC PLEXUS BLOCK CATHETER KIT receive FDA 510(k) clearance?

LOPER CELIAC PLEXUS BLOCK CATHETER KIT received FDA 510(k) clearance on 1990-02-22, under 510(k) number K895955.

Who is the listed applicant for LOPER CELIAC PLEXUS BLOCK CATHETER KIT?

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

What is the FDA product code for LOPER CELIAC PLEXUS BLOCK CATHETER KIT?

The FDA product code for LOPER CELIAC PLEXUS BLOCK CATHETER KIT is CAZ.

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Other records listing Opticon Medical, 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.

K033830OPTION-VF URINARY CATHETER WITH ADAPTOR, MODEL FVA14218; OPTION-V CONTINUOUS DRAINAGE ADAPTOR, MODEL CDA1000K023090OPTION-VF URINARY CATHETER, FV14218K970716OPTICON DIRECT MALE URINARY CATHETER FOR CONTINUOUS DRAINAGEK930194HEMOSTASIS VALVE AND TUBING SETK904999WEINGARTEN TM CAPNOGRAPHIC INTUBATION STYLETTEK895476OPTION EPIDURAL CATHETERS

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Related Devices (Code: CAZ)

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.

K261372Profoject™ LOR SyringeCMT Health PTE., Ltd.K222341Arrow 0.2 Micron Flat Filter, GVSArrow International, LLCK210983BD Epilor SyringeBecton, Dickinson and CompanyK201356Plastic LOR SyringeJiangsu Caina Medical Co.,LtdK202699E-Cath STIM acc. TsuiPAJUNK GmbH MedizintechnologieK190345VPCPAJUNK GmbH Medizintechnologie

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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