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FDA 510(k)

MORELL INJECTOR

K-Number: K951870 · 1996-01-22

ApplicantIncutech, Inc.
Decision Date1996-01-22
Product CodeCAZ
Advisory CommitteeAN
DecisionUnknown

Device Summary

MORELL INJECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Incutech, Inc.. It received FDA 510(k) clearance on 1996-01-22 under 510(k) number K951870. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MORELL INJECTOR?

MORELL INJECTOR is a medical device that received FDA 510(k) clearance on 1996-01-22. The listed applicant is Incutech, Inc.. The 510(k) number is K951870.

When did MORELL INJECTOR receive FDA 510(k) clearance?

MORELL INJECTOR received FDA 510(k) clearance on 1996-01-22, under 510(k) number K951870.

Who is the listed applicant for MORELL INJECTOR?

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

What is the FDA product code for MORELL INJECTOR?

The FDA product code for MORELL INJECTOR is CAZ.

Related Clinical Trials

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.

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Other records listing Incutech, 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.

K960619MORE-L INJECTOR KIT PLUSK942394SAFE VENT SYSTEMK941731EMPTY, SOLUTION TRANSFER CONTAINER WITH DETATCHABLE LEG SETK940258SOLUTION TRANSFER CONTAINER W/ATTACHED LEG SET (EMPTY)

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

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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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