FDA 510(k)

TONOTEST BLOOD PRESSURE DEVICE

K-Number: K790682 · 1979-04-11

Decision Date1979-04-11

Product Code

DecisionUnknown

Device Summary

TONOTEST BLOOD PRESSURE DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Robert Bosch Corp.. It received FDA 510(k) clearance on 1979-04-11 under 510(k) number K790682. FDA Decision: Unknown.

Frequently Asked Questions

What is the TONOTEST BLOOD PRESSURE DEVICE?

TONOTEST BLOOD PRESSURE DEVICE is a medical device that received FDA 510(k) clearance on 1979-04-11. The listed applicant is Robert Bosch Corp.. The 510(k) number is K790682.

When did TONOTEST BLOOD PRESSURE DEVICE receive FDA 510(k) clearance?

TONOTEST BLOOD PRESSURE DEVICE received FDA 510(k) clearance on 1979-04-11, under 510(k) number K790682.

Who is the listed applicant for TONOTEST BLOOD PRESSURE DEVICE?

The FDA 510(k) record lists Robert Bosch Corp. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Robert Bosch Corp. as applicant

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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.