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FDA 510(k)

WATERS 474 SCANNING FLOURESCENCE DETECTOR (474)

K-Number: K962574 · 1996-07-22

Decision Date1996-07-22
Product CodeLEQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

WATERS 474 SCANNING FLOURESCENCE DETECTOR (474) is the device name listed in this FDA 510(k) record. The listed applicant is Waters Corporation. It received FDA 510(k) clearance on 1996-07-22 under 510(k) number K962574. The device is classified under product code LEQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WATERS 474 SCANNING FLOURESCENCE DETECTOR (474)?

WATERS 474 SCANNING FLOURESCENCE DETECTOR (474) is a medical device that received FDA 510(k) clearance on 1996-07-22. The listed applicant is Waters Corporation. The 510(k) number is K962574.

When did WATERS 474 SCANNING FLOURESCENCE DETECTOR (474) receive FDA 510(k) clearance?

WATERS 474 SCANNING FLOURESCENCE DETECTOR (474) received FDA 510(k) clearance on 1996-07-22, under 510(k) number K962574.

Who is the listed applicant for WATERS 474 SCANNING FLOURESCENCE DETECTOR (474)?

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

What is the FDA product code for WATERS 474 SCANNING FLOURESCENCE DETECTOR (474)?

The FDA product code for WATERS 474 SCANNING FLOURESCENCE DETECTOR (474) is LEQ.

Related Clinical Trials

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.

Other records listing Waters Corporation 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.

Related Devices (Code: LEQ)

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.

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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