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FDA 510(k)

ENTREE BLUNT TIP TROCAR AND ADAPTER

K-Number: K932020 · 1994-01-11

ApplicantCore Dynamics, Inc.
Decision Date1994-01-11
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ENTREE BLUNT TIP TROCAR AND ADAPTER 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 1994-01-11 under 510(k) number K932020. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENTREE BLUNT TIP TROCAR AND ADAPTER?

ENTREE BLUNT TIP TROCAR AND ADAPTER is a medical device that received FDA 510(k) clearance on 1994-01-11. The listed applicant is Core Dynamics, Inc.. The 510(k) number is K932020.

When did ENTREE BLUNT TIP TROCAR AND ADAPTER receive FDA 510(k) clearance?

ENTREE BLUNT TIP TROCAR AND ADAPTER received FDA 510(k) clearance on 1994-01-11, under 510(k) number K932020.

Who is the listed applicant for ENTREE BLUNT TIP TROCAR AND ADAPTER?

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 BLUNT TIP TROCAR AND ADAPTER?

The FDA product code for ENTREE BLUNT TIP TROCAR AND ADAPTER is HET.

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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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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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