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FDA 510(k)

YANKAUER SUCTION INSTRU./LAYTEX GLOVES/SUCT. CATH.

K-Number: K881429 · 1988-04-25

ApplicantMedical Repackers Co.
Decision Date1988-04-25
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

YANKAUER SUCTION INSTRU./LAYTEX GLOVES/SUCT. CATH. is the device name listed in this FDA 510(k) record. The listed applicant is Medical Repackers Co.. It received FDA 510(k) clearance on 1988-04-25 under 510(k) number K881429. 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 YANKAUER SUCTION INSTRU./LAYTEX GLOVES/SUCT. CATH.?

YANKAUER SUCTION INSTRU./LAYTEX GLOVES/SUCT. CATH. is a medical device that received FDA 510(k) clearance on 1988-04-25. The listed applicant is Medical Repackers Co.. The 510(k) number is K881429.

When did YANKAUER SUCTION INSTRU./LAYTEX GLOVES/SUCT. CATH. receive FDA 510(k) clearance?

YANKAUER SUCTION INSTRU./LAYTEX GLOVES/SUCT. CATH. received FDA 510(k) clearance on 1988-04-25, under 510(k) number K881429.

Who is the listed applicant for YANKAUER SUCTION INSTRU./LAYTEX GLOVES/SUCT. CATH.?

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

What is the FDA product code for YANKAUER SUCTION INSTRU./LAYTEX GLOVES/SUCT. CATH.?

The FDA product code for YANKAUER SUCTION INSTRU./LAYTEX GLOVES/SUCT. CATH. is CAZ.

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Other records listing Medical Repackers Co. 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.

K890575ACCUTHERM PTS-200K882977ASK-300K881313IQK-200K874674AIK-100 ANESTHESIA INDUCTION KIT/TRAY

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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