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FDA 510(k)

FILLISCOPE

K-Number: K930804 · 1993-10-07

ApplicantFilliscope, Inc.
Decision Date1993-10-07
Product CodeCCW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FILLISCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Filliscope, Inc.. It received FDA 510(k) clearance on 1993-10-07 under 510(k) number K930804. The device is classified under product code CCW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FILLISCOPE?

FILLISCOPE is a medical device that received FDA 510(k) clearance on 1993-10-07. The listed applicant is Filliscope, Inc.. The 510(k) number is K930804.

When did FILLISCOPE receive FDA 510(k) clearance?

FILLISCOPE received FDA 510(k) clearance on 1993-10-07, under 510(k) number K930804.

Who is the listed applicant for FILLISCOPE?

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

What is the FDA product code for FILLISCOPE?

The FDA product code for FILLISCOPE is CCW.

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Related Devices (Code: CCW)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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