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FDA 510(k)

HTSH RIA

K-Number: K780122 · 1978-02-03

ApplicantAbbott Laboratories
Decision Date1978-02-03
Product CodeKHO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

HTSH RIA is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1978-02-03 under 510(k) number K780122. The device is classified under product code KHO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HTSH RIA?

HTSH RIA is a medical device that received FDA 510(k) clearance on 1978-02-03. The listed applicant is Abbott Laboratories. The 510(k) number is K780122.

When did HTSH RIA receive FDA 510(k) clearance?

HTSH RIA received FDA 510(k) clearance on 1978-02-03, under 510(k) number K780122.

Who is the listed applicant for HTSH RIA?

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

What is the FDA product code for HTSH RIA?

The FDA product code for HTSH RIA is KHO.

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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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