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FDA 510(k)

DOPCORD PPG

K-Number: K884451 · 1989-01-12

ApplicantHuntleigh Technology, Inc.
Decision Date1989-01-12
Product CodeJOM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DOPCORD PPG is the device name listed in this FDA 510(k) record. The listed applicant is Huntleigh Technology, Inc.. It received FDA 510(k) clearance on 1989-01-12 under 510(k) number K884451. The device is classified under product code JOM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOPCORD PPG?

DOPCORD PPG is a medical device that received FDA 510(k) clearance on 1989-01-12. The listed applicant is Huntleigh Technology, Inc.. The 510(k) number is K884451.

When did DOPCORD PPG receive FDA 510(k) clearance?

DOPCORD PPG received FDA 510(k) clearance on 1989-01-12, under 510(k) number K884451.

Who is the listed applicant for DOPCORD PPG?

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

What is the FDA product code for DOPCORD PPG?

The FDA product code for DOPCORD PPG is JOM.

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Other records listing Huntleigh Technology, Inc. as applicant

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

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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