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FDA 510(k)

MT9000 CHART RECORDER

K-Number: K892067 · 1989-06-05

ApplicantAstro-Med, Inc.
Decision Date1989-06-05
Product CodeDSH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MT9000 CHART RECORDER is the device name listed in this FDA 510(k) record. The listed applicant is Astro-Med, Inc.. It received FDA 510(k) clearance on 1989-06-05 under 510(k) number K892067. The device is classified under product code DSH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MT9000 CHART RECORDER?

MT9000 CHART RECORDER is a medical device that received FDA 510(k) clearance on 1989-06-05. The listed applicant is Astro-Med, Inc.. The 510(k) number is K892067.

When did MT9000 CHART RECORDER receive FDA 510(k) clearance?

MT9000 CHART RECORDER received FDA 510(k) clearance on 1989-06-05, under 510(k) number K892067.

Who is the listed applicant for MT9000 CHART RECORDER?

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

What is the FDA product code for MT9000 CHART RECORDER?

The FDA product code for MT9000 CHART RECORDER is DSH.

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Other records listing Astro-Med, Inc. as applicant

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Related Devices (Code: DSH)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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