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FDA 510(k)

THE HOMMED SENTRY, MODEL 1 SENTRY

K-Number: K993938 · 2000-03-15

ApplicantHommed, LLC
Decision Date2000-03-15
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

THE HOMMED SENTRY, MODEL 1 SENTRY is the device name listed in this FDA 510(k) record. The listed applicant is Hommed, LLC. It received FDA 510(k) clearance on 2000-03-15 under 510(k) number K993938. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE HOMMED SENTRY, MODEL 1 SENTRY?

THE HOMMED SENTRY, MODEL 1 SENTRY is a medical device that received FDA 510(k) clearance on 2000-03-15. The listed applicant is Hommed, LLC. The 510(k) number is K993938.

When did THE HOMMED SENTRY, MODEL 1 SENTRY receive FDA 510(k) clearance?

THE HOMMED SENTRY, MODEL 1 SENTRY received FDA 510(k) clearance on 2000-03-15, under 510(k) number K993938.

Who is the listed applicant for THE HOMMED SENTRY, MODEL 1 SENTRY?

The FDA 510(k) record lists Hommed, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE HOMMED SENTRY, MODEL 1 SENTRY?

The FDA product code for THE HOMMED SENTRY, MODEL 1 SENTRY is DXN.

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Other records listing Hommed, LLC as applicant

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.

K040799HOMMED GENESIS PATIENT MONITOR SYSTEM WITH OPTIONSK040651HOMMED SENTRY IIIB-F PATIENT MONITOR SYSTEMK040032CENTRAL STATION, VERSION 3.3HK020184HOMMED CENTRAL STATIONK014025HOMMED SENTRY III PATIENT MONITOR SYSTEM WITH CARD READERK003180HOMMED OBSERVER, MODEL I

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Related Devices (Code: DXN)

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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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