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FDA 510(k)

NEOLINE(TM)

K-Number: K914778 · 1992-09-16

ApplicantMartech Medical Products, Inc.
Decision Date1992-09-16
Product CodeCBT
Advisory CommitteeAN
DecisionUnknown

Device Summary

NEOLINE(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Martech Medical Products, Inc.. It received FDA 510(k) clearance on 1992-09-16 under 510(k) number K914778. The device is classified under product code CBT. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the NEOLINE(TM)?

NEOLINE(TM) is a medical device that received FDA 510(k) clearance on 1992-09-16. The listed applicant is Martech Medical Products, Inc.. The 510(k) number is K914778.

When did NEOLINE(TM) receive FDA 510(k) clearance?

NEOLINE(TM) received FDA 510(k) clearance on 1992-09-16, under 510(k) number K914778.

Who is the listed applicant for NEOLINE(TM)?

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

What is the FDA product code for NEOLINE(TM)?

The FDA product code for NEOLINE(TM) is CBT.

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Other records listing Martech Medical Products, 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.

K960519MARTECH ENDOSCOPIC INJECTION NEEDLEK931924MARKSMAN ARTERIAL BLOOD GAS SYRINGEK922438PRO2 OXYGEN ANALYZERK926007ACCESSORY TO PISTON SYRINGEK910970MARKSMAN ARTERIAL BLOOD GAS SYRINGEK890473NEEDLE GUARD(TM)

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Related Devices (Code: CBT)

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.

K071269HEMODRAW ARTERIAL BLOOD SAMPLING SYSTEMSmiths Medical Asd, Inc.K070340SECURE ARTERIAL BLOOD SAMPLING SYSTEMSmiths Medical Asd, Inc.K955663ABC IN-LINE BLOOD SAMPLING KITUtah Medical Products, Inc.K954015ABG POINT LOK NEEDLE PROTECTION DEVICEDevon Industries, Inc.K954035ACTI-FLEX ARTERIAL EXTENSION SETR-Group Intl.K950098NEEDLE SAFETY COVERHammer-Plane, Inc.

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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