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FDA 510(k)

FUJINON EVL-F (TENTATIVE) AND TROCAR

K-Number: K902197 · 1991-03-05

ApplicantFujinon, Inc.
Decision Date1991-03-05
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FUJINON EVL-F (TENTATIVE) AND TROCAR is the device name listed in this FDA 510(k) record. The listed applicant is Fujinon, Inc.. It received FDA 510(k) clearance on 1991-03-05 under 510(k) number K902197. 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 FUJINON EVL-F (TENTATIVE) AND TROCAR?

FUJINON EVL-F (TENTATIVE) AND TROCAR is a medical device that received FDA 510(k) clearance on 1991-03-05. The listed applicant is Fujinon, Inc.. The 510(k) number is K902197.

When did FUJINON EVL-F (TENTATIVE) AND TROCAR receive FDA 510(k) clearance?

FUJINON EVL-F (TENTATIVE) AND TROCAR received FDA 510(k) clearance on 1991-03-05, under 510(k) number K902197.

Who is the listed applicant for FUJINON EVL-F (TENTATIVE) AND TROCAR?

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

What is the FDA product code for FUJINON EVL-F (TENTATIVE) AND TROCAR?

The FDA product code for FUJINON EVL-F (TENTATIVE) AND TROCAR is HET.

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Other records listing Fujinon, Inc. as applicant

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Related Devices (Code: HET)

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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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