FDA 510(k)

HTS *1

K-Number: K822843 · 1982-12-15

ApplicantGlobal Office Automation System, Inc.

Decision Date1982-12-15

Product CodeDSK

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

HTS *1 is the device name listed in this FDA 510(k) record. The listed applicant is Global Office Automation System, Inc.. It received FDA 510(k) clearance on 1982-12-15 under 510(k) number K822843. The device is classified under product code DSK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HTS *1?

HTS *1 is a medical device that received FDA 510(k) clearance on 1982-12-15. The listed applicant is Global Office Automation System, Inc.. The 510(k) number is K822843.

When did HTS *1 receive FDA 510(k) clearance?

HTS *1 received FDA 510(k) clearance on 1982-12-15, under 510(k) number K822843.

Who is the listed applicant for HTS *1?

The FDA 510(k) record lists Global Office Automation System, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HTS *1?

The FDA product code for HTS *1 is DSK.

Related Devices (Code: DSK)

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.

K231586Endophys Blood Pressure Monitor model BPM-30Endophys Technologies, LLC K160945Endophys Blood Pressure MonitorEndophys Holdings, LLC K080670MODIFICATION TO SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEMAtcor Medical K070795SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEMAtcor Medical Pty, Ltd.K033738MONITORING SYSTEM, MODEL ARGUS PB-2200Schiller AG K021517ABP FOR WINDOWSRozinn Electronics, Inc.

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.