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FDA 510(k)

MICRO TRANSDUCER CATHETERS

K-Number: K813125 · 1981-12-14

ApplicantHoneywell, Inc.
Decision Date1981-12-14
Product CodeDRE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICRO TRANSDUCER CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1981-12-14 under 510(k) number K813125. The device is classified under product code DRE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO TRANSDUCER CATHETERS?

MICRO TRANSDUCER CATHETERS is a medical device that received FDA 510(k) clearance on 1981-12-14. The listed applicant is Honeywell, Inc.. The 510(k) number is K813125.

When did MICRO TRANSDUCER CATHETERS receive FDA 510(k) clearance?

MICRO TRANSDUCER CATHETERS received FDA 510(k) clearance on 1981-12-14, under 510(k) number K813125.

Who is the listed applicant for MICRO TRANSDUCER CATHETERS?

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

What is the FDA product code for MICRO TRANSDUCER CATHETERS?

The FDA product code for MICRO TRANSDUCER CATHETERS is DRE.

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Other records listing Honeywell, Inc. as applicant

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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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