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FDA 510(k)

MULTI-CAVITY EQUILIBRIUM CELL

K-Number: K771434 · 1977-08-22

ApplicantTechhnilab Instruments, Inc.
Decision Date1977-08-22
Product Code
DecisionSubstantially Equivalent

Device Summary

MULTI-CAVITY EQUILIBRIUM CELL is the device name listed in this FDA 510(k) record. The listed applicant is Techhnilab Instruments, Inc.. It received FDA 510(k) clearance on 1977-08-22 under 510(k) number K771434. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-CAVITY EQUILIBRIUM CELL?

MULTI-CAVITY EQUILIBRIUM CELL is a medical device that received FDA 510(k) clearance on 1977-08-22. The listed applicant is Techhnilab Instruments, Inc.. The 510(k) number is K771434.

When did MULTI-CAVITY EQUILIBRIUM CELL receive FDA 510(k) clearance?

MULTI-CAVITY EQUILIBRIUM CELL received FDA 510(k) clearance on 1977-08-22, under 510(k) number K771434.

Who is the listed applicant for MULTI-CAVITY EQUILIBRIUM CELL?

The FDA 510(k) record lists Techhnilab Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Techhnilab Instruments, Inc. 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.

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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.

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