Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PICOSCALE LABORSCALE, #PSL-1 & ANALYSER, #PSA-1

K-Number: K853036 · 1985-11-05

ApplicantDiagnostic Technology, Inc.
Decision Date1985-11-05
Product CodeGKL
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

PICOSCALE LABORSCALE, #PSL-1 & ANALYSER, #PSA-1 is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Technology, Inc.. It received FDA 510(k) clearance on 1985-11-05 under 510(k) number K853036. 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 PICOSCALE LABORSCALE, #PSL-1 & ANALYSER, #PSA-1?

PICOSCALE LABORSCALE, #PSL-1 & ANALYSER, #PSA-1 is a medical device that received FDA 510(k) clearance on 1985-11-05. The listed applicant is Diagnostic Technology, Inc.. The 510(k) number is K853036.

When did PICOSCALE LABORSCALE, #PSL-1 & ANALYSER, #PSA-1 receive FDA 510(k) clearance?

PICOSCALE LABORSCALE, #PSL-1 & ANALYSER, #PSA-1 received FDA 510(k) clearance on 1985-11-05, under 510(k) number K853036.

Who is the listed applicant for PICOSCALE LABORSCALE, #PSL-1 & ANALYSER, #PSA-1?

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

What is the FDA product code for PICOSCALE LABORSCALE, #PSL-1 & ANALYSER, #PSA-1?

The FDA product code for PICOSCALE LABORSCALE, #PSL-1 & ANALYSER, #PSA-1 is GKL.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Diagnostic Technology, Inc. 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.

K896378LYME-CHECK(TM) TEST KITK903612EBV/EA-CHECK TM TEST KITK891542EBNA-CHECK(TM) TEST KITK890819HSV-CHECK(TM) TEST KITK890639RESUBMITTED EBV/IGM-CHECK TEST KITK871373EBV-CHECK(TM) TEST KIT (IGG)

View all 28 devices →

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.

↑