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FDA 510(k)

TREND II ANEROID

K-Number: K780598 · 1978-06-06

ApplicantAbco Dealers, Inc.
Decision Date1978-06-06
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TREND II ANEROID is the device name listed in this FDA 510(k) record. The listed applicant is Abco Dealers, Inc.. It received FDA 510(k) clearance on 1978-06-06 under 510(k) number K780598. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TREND II ANEROID?

TREND II ANEROID is a medical device that received FDA 510(k) clearance on 1978-06-06. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K780598.

When did TREND II ANEROID receive FDA 510(k) clearance?

TREND II ANEROID received FDA 510(k) clearance on 1978-06-06, under 510(k) number K780598.

Who is the listed applicant for TREND II ANEROID?

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

What is the FDA product code for TREND II ANEROID?

The FDA product code for TREND II ANEROID is DXN.

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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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