OWENS TROCAR
K-Number: K932796 · 1994-02-02
Advertisement
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement