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FDA 510(k)

HAMILTON-THORN MOTILITY ANALYZER HTM-2000

K-Number: K873172 · 1987-11-06

ApplicantHamilton Thorne Research
Decision Date1987-11-06
Product CodeGKL
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

HAMILTON-THORN MOTILITY ANALYZER HTM-2000 is the device name listed in this FDA 510(k) record. The listed applicant is Hamilton Thorne Research. It received FDA 510(k) clearance on 1987-11-06 under 510(k) number K873172. The device is classified under product code GKL. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAMILTON-THORN MOTILITY ANALYZER HTM-2000?

HAMILTON-THORN MOTILITY ANALYZER HTM-2000 is a medical device that received FDA 510(k) clearance on 1987-11-06. The listed applicant is Hamilton Thorne Research. The 510(k) number is K873172.

When did HAMILTON-THORN MOTILITY ANALYZER HTM-2000 receive FDA 510(k) clearance?

HAMILTON-THORN MOTILITY ANALYZER HTM-2000 received FDA 510(k) clearance on 1987-11-06, under 510(k) number K873172.

Who is the listed applicant for HAMILTON-THORN MOTILITY ANALYZER HTM-2000?

The FDA 510(k) record lists Hamilton Thorne Research as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HAMILTON-THORN MOTILITY ANALYZER HTM-2000?

The FDA product code for HAMILTON-THORN MOTILITY ANALYZER HTM-2000 is GKL.

Related Clinical Trials

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Other records listing Hamilton Thorne Research 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.

K012805AUTOMARQERK000380FOTOMASTERK990184AUTOMARQERK920719IVOS ANALYZER

Related Devices (Code: GKL)

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.

K152776Glocyte Automated Cell Counter SystemAdvanced Instruments, Inc.K091539IQ 200 URINE ANALIZER BODY FLUIDS MODULEIris DiagnosticsK071652HEMOCUE WBC SYSTEMHemocue ABK051693MODIFICATION TO BAYER ADVIA 2120 HEMATOLOGY ANALYZER WITH AUTOSLIDE SYSTEMBayer Healthcare, LLCK050235IQ 200 URINE ANALYZER BODY FLUIDS MODULEIris International, Inc.K032677SYSMEX POCH-100ISysmex America, Inc.

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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