Cleared Traditional

K790682 - TONOTEST BLOOD PRESSURE DEVICE

K790682 · Robert Bosch Corp. · Cardiovascular device
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Apr 1979
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K790682 is an FDA 510(k) clearance for the TONOTEST BLOOD PRESSURE DEVICE.

Submitted by Robert Bosch Corp. (Mchenry, US). The FDA issued a Cleared decision on April 11, 1979.

This device falls under the Cardiovascular FDA review panel. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Cardiovascular review framework, consistent with the majority of Class II 510(k) submissions.

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FDA 510(k) Submission Details - K790682

510(k) Number K790682 FDA.gov
FDA Decision Cleared Substantially Equivalent - Product Development Protocol (SESP)
Date Received April 11, 1979
Decision Date April 11, 1979
Days to Decision -
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Pathway characteristics
Predicate-based equivalence.

Device Classification - Class ,

Product Code -
Device Class -