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FDA 510(k)

RECORD, MODEL 702, I.L.

K-Number: K770946 · 1977-07-05

ApplicantInstrumentation Laboratory CO
Decision Date1977-07-05
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RECORD, MODEL 702, I.L. 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 1977-07-05 under 510(k) number K770946. The device is classified under product code DSF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RECORD, MODEL 702, I.L.?

RECORD, MODEL 702, I.L. is a medical device that received FDA 510(k) clearance on 1977-07-05. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K770946.

When did RECORD, MODEL 702, I.L. receive FDA 510(k) clearance?

RECORD, MODEL 702, I.L. received FDA 510(k) clearance on 1977-07-05, under 510(k) number K770946.

Who is the listed applicant for RECORD, MODEL 702, I.L.?

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 RECORD, MODEL 702, I.L.?

The FDA product code for RECORD, MODEL 702, I.L. is DSF.

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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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