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FDA 510(k)

DYE CURVE EVALUATOR

K-Number: K792135 · 1980-01-11

ApplicantSci-Pro, Inc.
Decision Date1980-01-11
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DYE CURVE EVALUATOR is the device name listed in this FDA 510(k) record. The listed applicant is Sci-Pro, Inc.. It received FDA 510(k) clearance on 1980-01-11 under 510(k) number K792135. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYE CURVE EVALUATOR?

DYE CURVE EVALUATOR is a medical device that received FDA 510(k) clearance on 1980-01-11. The listed applicant is Sci-Pro, Inc.. The 510(k) number is K792135.

When did DYE CURVE EVALUATOR receive FDA 510(k) clearance?

DYE CURVE EVALUATOR received FDA 510(k) clearance on 1980-01-11, under 510(k) number K792135.

Who is the listed applicant for DYE CURVE EVALUATOR?

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

What is the FDA product code for DYE CURVE EVALUATOR?

The FDA product code for DYE CURVE EVALUATOR is DQK.

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Related Devices (Code: DQK)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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