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FDA 510(k)

FLYNN TISSUE PROBE AND BLUNT DISSECTOR

K-Number: K910713 · 1991-03-21

ApplicantMarlo Surgical Technology
Decision Date1991-03-21
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FLYNN TISSUE PROBE AND BLUNT DISSECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Marlo Surgical Technology. It received FDA 510(k) clearance on 1991-03-21 under 510(k) number K910713. 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 FLYNN TISSUE PROBE AND BLUNT DISSECTOR?

FLYNN TISSUE PROBE AND BLUNT DISSECTOR is a medical device that received FDA 510(k) clearance on 1991-03-21. The listed applicant is Marlo Surgical Technology. The 510(k) number is K910713.

When did FLYNN TISSUE PROBE AND BLUNT DISSECTOR receive FDA 510(k) clearance?

FLYNN TISSUE PROBE AND BLUNT DISSECTOR received FDA 510(k) clearance on 1991-03-21, under 510(k) number K910713.

Who is the listed applicant for FLYNN TISSUE PROBE AND BLUNT DISSECTOR?

The FDA 510(k) record lists Marlo Surgical Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLYNN TISSUE PROBE AND BLUNT DISSECTOR?

The FDA product code for FLYNN TISSUE PROBE AND BLUNT DISSECTOR is HET.

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Other records listing Marlo Surgical Technology 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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