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FDA 510(k)

SPECTROPHOTOMETER, MODEL 751

K-Number: K770645 · 1977-06-24

ApplicantInstrumentation Laboratory CO
Decision Date1977-06-24
Product CodeJXR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SPECTROPHOTOMETER, MODEL 751 is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory CO. It received FDA 510(k) clearance on 1977-06-24 under 510(k) number K770645. The device is classified under product code JXR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPECTROPHOTOMETER, MODEL 751?

SPECTROPHOTOMETER, MODEL 751 is a medical device that received FDA 510(k) clearance on 1977-06-24. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K770645.

When did SPECTROPHOTOMETER, MODEL 751 receive FDA 510(k) clearance?

SPECTROPHOTOMETER, MODEL 751 received FDA 510(k) clearance on 1977-06-24, under 510(k) number K770645.

Who is the listed applicant for SPECTROPHOTOMETER, MODEL 751?

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

What is the FDA product code for SPECTROPHOTOMETER, MODEL 751?

The FDA product code for SPECTROPHOTOMETER, MODEL 751 is JXR.

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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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