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FDA 510(k)

LIFE WATCH LSI

K-Number: K822615 · 1982-09-21

ApplicantLife Science Instrumentation, Inc.
Decision Date1982-09-21
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIFE WATCH LSI 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 1982-09-21 under 510(k) number K822615. 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 LIFE WATCH LSI?

LIFE WATCH LSI is a medical device that received FDA 510(k) clearance on 1982-09-21. The listed applicant is Life Science Instrumentation, Inc.. The 510(k) number is K822615.

When did LIFE WATCH LSI receive FDA 510(k) clearance?

LIFE WATCH LSI received FDA 510(k) clearance on 1982-09-21, under 510(k) number K822615.

Who is the listed applicant for LIFE WATCH LSI?

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 LIFE WATCH LSI?

The FDA product code for LIFE WATCH LSI 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.

K254058DistaSense(TM) (v1)Life Detection TechnologiesK261286The Circadia C300 System (C300)Circadia Health, Inc.K252676The Circadia C300 System (C300)Circadia Health, Inc.K253388Sleepiz One+ (Model 2.5)Sleepiz AGK251364Sleepiz One+ (2.5)Sleepiz AGK234003The Circadia C200 SystemCircadia Technologies, Ltd.

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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