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FDA 510(k)

ZEE EXTRICATION DEVICE

K-Number: K812342 · 1981-09-21

ApplicantZee Medical Products Co., Inc.
Decision Date1981-09-21
Product CodeIQF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ZEE EXTRICATION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Zee Medical Products Co., Inc.. It received FDA 510(k) clearance on 1981-09-21 under 510(k) number K812342. The device is classified under product code IQF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZEE EXTRICATION DEVICE?

ZEE EXTRICATION DEVICE is a medical device that received FDA 510(k) clearance on 1981-09-21. The listed applicant is Zee Medical Products Co., Inc.. The 510(k) number is K812342.

When did ZEE EXTRICATION DEVICE receive FDA 510(k) clearance?

ZEE EXTRICATION DEVICE received FDA 510(k) clearance on 1981-09-21, under 510(k) number K812342.

Who is the listed applicant for ZEE EXTRICATION DEVICE?

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

What is the FDA product code for ZEE EXTRICATION DEVICE?

The FDA product code for ZEE EXTRICATION DEVICE is IQF.

Related Clinical Trials

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Other records listing Zee Medical Products Co., 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.

K823501ZEE SPHYGMOMANOMETERK813156ULTRA-WIDE SAFETY SPECTACLE FRAMEK813016ZEE TRACTION SPLINTK812814ZEE SURGICAL INSTRUMENTSK812564ZEE LIFE SUPPORT AIR PANTSK812284ZEE ELECTRODE-GEL

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Related Devices (Code: IQF)

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.

K832741JASON CERVICAL ORTHOSISOrthomedicsK811297CERVICAL SUPPORTOrthomedicsK810555SCOLIOSIS ORTHOTIC SYSTEMOrthomedicsK791350POPE AMBULATORY HALO VESTHospital Products Co.K781761KENDRICK EXTRICATION DEVICEMedi-Ked, Inc.K780489SPINE BOARDMarullo, Baldwin, Frieden, Gatewood,

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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