FDA 510(k)

CYSTIC FIBROSIS TESTING INSTRUMENT

K-Number: K772176 · 1977-12-20

ApplicantLaboratory Equipment Design Co.

Decision Date1977-12-20

Product CodeJJN

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

CYSTIC FIBROSIS TESTING INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Laboratory Equipment Design Co.. It received FDA 510(k) clearance on 1977-12-20 under 510(k) number K772176. The device is classified under product code JJN. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYSTIC FIBROSIS TESTING INSTRUMENT?

CYSTIC FIBROSIS TESTING INSTRUMENT is a medical device that received FDA 510(k) clearance on 1977-12-20. The listed applicant is Laboratory Equipment Design Co.. The 510(k) number is K772176.

When did CYSTIC FIBROSIS TESTING INSTRUMENT receive FDA 510(k) clearance?

CYSTIC FIBROSIS TESTING INSTRUMENT received FDA 510(k) clearance on 1977-12-20, under 510(k) number K772176.

Who is the listed applicant for CYSTIC FIBROSIS TESTING INSTRUMENT?

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

What is the FDA product code for CYSTIC FIBROSIS TESTING INSTRUMENT?

The FDA product code for CYSTIC FIBROSIS TESTING INSTRUMENT is JJN.

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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.