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FDA 510(k)

FURNACE AUTOSAMPLER, MODEL 155

K-Number: K770994 · 1977-08-22

ApplicantInstrumentation Laboratory CO
Decision Date1977-08-22
Product CodeDOP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FURNACE AUTOSAMPLER, MODEL 155 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 1977-08-22 under 510(k) number K770994. The device is classified under product code DOP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FURNACE AUTOSAMPLER, MODEL 155?

FURNACE AUTOSAMPLER, MODEL 155 is a medical device that received FDA 510(k) clearance on 1977-08-22. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K770994.

When did FURNACE AUTOSAMPLER, MODEL 155 receive FDA 510(k) clearance?

FURNACE AUTOSAMPLER, MODEL 155 received FDA 510(k) clearance on 1977-08-22, under 510(k) number K770994.

Who is the listed applicant for FURNACE AUTOSAMPLER, MODEL 155?

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 FURNACE AUTOSAMPLER, MODEL 155?

The FDA product code for FURNACE AUTOSAMPLER, MODEL 155 is DOP.

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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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