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FDA 510(k)

ZEE SURGICAL INSTRUMENTS

K-Number: K812814 · 1981-11-06

Decision Date1981-11-06
Product CodeGDZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ZEE SURGICAL INSTRUMENTS 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 1981-11-06 under 510(k) number K812814. The device is classified under product code GDZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZEE SURGICAL INSTRUMENTS?

ZEE SURGICAL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1981-11-06. The listed applicant is Zee Medical Products Co., Inc.. The 510(k) number is K812814.

When did ZEE SURGICAL INSTRUMENTS receive FDA 510(k) clearance?

ZEE SURGICAL INSTRUMENTS received FDA 510(k) clearance on 1981-11-06, under 510(k) number K812814.

Who is the listed applicant for ZEE SURGICAL INSTRUMENTS?

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 SURGICAL INSTRUMENTS?

The FDA product code for ZEE SURGICAL INSTRUMENTS is GDZ.

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.

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.

View all 8 devices →

Related Devices (Code: GDZ)

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.

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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