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FDA 510(k)

TELEMANOMETER

K-Number: K850166 · 1985-04-18

ApplicantR.J. Ash, Medical Monitoring, Inc.
Decision Date1985-04-18
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TELEMANOMETER is the device name listed in this FDA 510(k) record. The listed applicant is R.J. Ash, Medical Monitoring, Inc.. It received FDA 510(k) clearance on 1985-04-18 under 510(k) number K850166. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TELEMANOMETER?

TELEMANOMETER is a medical device that received FDA 510(k) clearance on 1985-04-18. The listed applicant is R.J. Ash, Medical Monitoring, Inc.. The 510(k) number is K850166.

When did TELEMANOMETER receive FDA 510(k) clearance?

TELEMANOMETER received FDA 510(k) clearance on 1985-04-18, under 510(k) number K850166.

Who is the listed applicant for TELEMANOMETER?

The FDA 510(k) record lists R.J. Ash, Medical Monitoring, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TELEMANOMETER?

The FDA product code for TELEMANOMETER is DRG.

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Related Devices (Code: DRG)

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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