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FDA 510(k)

DUAL COMPONENT STANDARDS

K-Number: K781423 · 1978-08-31

ApplicantAbbott Laboratories
Decision Date1978-08-31
Product CodeJIT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DUAL COMPONENT STANDARDS is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1978-08-31 under 510(k) number K781423. The device is classified under product code JIT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUAL COMPONENT STANDARDS?

DUAL COMPONENT STANDARDS is a medical device that received FDA 510(k) clearance on 1978-08-31. The listed applicant is Abbott Laboratories. The 510(k) number is K781423.

When did DUAL COMPONENT STANDARDS receive FDA 510(k) clearance?

DUAL COMPONENT STANDARDS received FDA 510(k) clearance on 1978-08-31, under 510(k) number K781423.

Who is the listed applicant for DUAL COMPONENT STANDARDS?

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 DUAL COMPONENT STANDARDS?

The FDA product code for DUAL COMPONENT STANDARDS is JIT.

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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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