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FDA 510(k)

OWENS TROCAR

K-Number: K932796 · 1994-02-02

Decision Date1994-02-02
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

OWENS TROCAR is the device name listed in this FDA 510(k) record. The listed applicant is Owens Industries, Inc.. It received FDA 510(k) clearance on 1994-02-02 under 510(k) number K932796. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OWENS TROCAR?

OWENS TROCAR is a medical device that received FDA 510(k) clearance on 1994-02-02. The listed applicant is Owens Industries, Inc.. The 510(k) number is K932796.

When did OWENS TROCAR receive FDA 510(k) clearance?

OWENS TROCAR received FDA 510(k) clearance on 1994-02-02, under 510(k) number K932796.

Who is the listed applicant for OWENS TROCAR?

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

What is the FDA product code for OWENS TROCAR?

The FDA product code for OWENS TROCAR is GCJ.

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 Owens Industries, 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.

Related Devices (Code: GCJ)

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

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