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FDA 510(k)

BIOSONICS SALIVARY TESTER

K-Number: K833635 · 1984-02-27

Decision Date1984-02-27
Product Code
DecisionSubstantially Equivalent

Device Summary

BIOSONICS SALIVARY TESTER is the device name listed in this FDA 510(k) record. The listed applicant is Meyer, Faller & Weisman. It received FDA 510(k) clearance on 1984-02-27 under 510(k) number K833635. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOSONICS SALIVARY TESTER?

BIOSONICS SALIVARY TESTER is a medical device that received FDA 510(k) clearance on 1984-02-27. The listed applicant is Meyer, Faller & Weisman. The 510(k) number is K833635.

When did BIOSONICS SALIVARY TESTER receive FDA 510(k) clearance?

BIOSONICS SALIVARY TESTER received FDA 510(k) clearance on 1984-02-27, under 510(k) number K833635.

Who is the listed applicant for BIOSONICS SALIVARY TESTER?

The FDA 510(k) record lists Meyer, Faller & Weisman as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

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.

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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