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FDA 510(k)

CENTERAL MONITOR 360

K-Number: K812144 · 1981-09-25

ApplicantLife Science Instrumentation, Inc.
Decision Date1981-09-25
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CENTERAL MONITOR 360 is the device name listed in this FDA 510(k) record. The listed applicant is Life Science Instrumentation, Inc.. It received FDA 510(k) clearance on 1981-09-25 under 510(k) number K812144. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTERAL MONITOR 360?

CENTERAL MONITOR 360 is a medical device that received FDA 510(k) clearance on 1981-09-25. The listed applicant is Life Science Instrumentation, Inc.. The 510(k) number is K812144.

When did CENTERAL MONITOR 360 receive FDA 510(k) clearance?

CENTERAL MONITOR 360 received FDA 510(k) clearance on 1981-09-25, under 510(k) number K812144.

Who is the listed applicant for CENTERAL MONITOR 360?

The FDA 510(k) record lists Life Science Instrumentation, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CENTERAL MONITOR 360?

The FDA product code for CENTERAL MONITOR 360 is DRT.

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Other records listing Life Science Instrumentation, Inc. as applicant

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Related Devices (Code: DRT)

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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