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)

LIQUID CHEMISTRY CONTROL, LEVEL I

K-Number: K870684 · 1987-04-06

ApplicantU. S. Diagnostics, Inc.
Decision Date1987-04-06
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIQUID CHEMISTRY CONTROL, LEVEL I is the device name listed in this FDA 510(k) record. The listed applicant is U. S. Diagnostics, Inc.. It received FDA 510(k) clearance on 1987-04-06 under 510(k) number K870684. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUID CHEMISTRY CONTROL, LEVEL I?

LIQUID CHEMISTRY CONTROL, LEVEL I is a medical device that received FDA 510(k) clearance on 1987-04-06. The listed applicant is U. S. Diagnostics, Inc.. The 510(k) number is K870684.

When did LIQUID CHEMISTRY CONTROL, LEVEL I receive FDA 510(k) clearance?

LIQUID CHEMISTRY CONTROL, LEVEL I received FDA 510(k) clearance on 1987-04-06, under 510(k) number K870684.

Who is the listed applicant for LIQUID CHEMISTRY CONTROL, LEVEL I?

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

What is the FDA product code for LIQUID CHEMISTRY CONTROL, LEVEL I?

The FDA product code for LIQUID CHEMISTRY CONTROL, LEVEL I is JJY.

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 U. S. Diagnostics, 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.

K110435EASYGLUCO PLUS BLOOD GLUCOSE MONITORING SYSTEMK082201G5 INFINITY BLODO GLUCOSE MONITORING SYSTEM WITH MODEL IGM, 0024AK061431EASYGLUCO, MODEL IGM-0002 G2K051651G4, MODEL IGM-0004K870596PROTHROMBIN TIME TESTK870685COAGULATION CONTROL, LEVEL I

View all 22 devices →

Related Devices (Code: JJY)

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.

K162530Multichem IA PlusTechno-Path ManufacturingK163629Audit MicroControls Linearity FD Tumor Markers IIAalto Scientific, Ltd.K163015Liquichek Tumor Marker Control-Level 1; Liquichek Tumor Marker Control-Level 2; Liquichek Tumor Marker Control-Level 3; Liquichek Tumor Marker Control- Trilevel MiniPakBio-Rad LaboratoriesK153712VK-3 Verification Kit, VK-4 Verification Kit, VK-R5 Verification Kit, VK-R7 Verification Kit, VK-Crea Verification KitRadiometer America, Inc.K132227LIQUICHEK IMMUNOASSAY PREMIUM CONTROL-TRILEVEL, LIQUICHEK IMMUNOASSAY PREMIUM CONTROL-LEVEL I, LIQUICHEK IMMUNOASSAYBio-Rad LaboratoriesK132156RANDOX CSF CONTROLS LEVELS 2 AND 3Randox Laboratories, 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.

↑