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FDA 510(k)

ENTREE THORACOSCOPY CANNULA SET

K-Number: K932022 · 1993-07-28

ApplicantCore Dynamics, Inc.
Decision Date1993-07-28
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENTREE THORACOSCOPY CANNULA SET is the device name listed in this FDA 510(k) record. The listed applicant is Core Dynamics, Inc.. It received FDA 510(k) clearance on 1993-07-28 under 510(k) number K932022. 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 ENTREE THORACOSCOPY CANNULA SET?

ENTREE THORACOSCOPY CANNULA SET is a medical device that received FDA 510(k) clearance on 1993-07-28. The listed applicant is Core Dynamics, Inc.. The 510(k) number is K932022.

When did ENTREE THORACOSCOPY CANNULA SET receive FDA 510(k) clearance?

ENTREE THORACOSCOPY CANNULA SET received FDA 510(k) clearance on 1993-07-28, under 510(k) number K932022.

Who is the listed applicant for ENTREE THORACOSCOPY CANNULA SET?

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

What is the FDA product code for ENTREE THORACOSCOPY CANNULA SET?

The FDA product code for ENTREE THORACOSCOPY CANNULA SET is GCJ.

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Other records listing Core Dynamics, 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.

K992250CORE AUDIBLE TROCAR IIK992190CORE POUCHK955490LAPAROSCOPIC KNITTERK953903LAPAROSCOPIC TROCAR OBTURATOR, 5MM, 10/11MM, 10/12MMK953409LAPAROSCOPIC TROCARK950457CANNUAL AND TROCAR, SUPERPUBIC

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Related Devices (Code: GCJ)

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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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