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)

SMS GLUCOSE CONTROL, MODEL 2120059

K-Number: K071433 · 2007-06-28

ApplicantSpecialty Medical Supplies
Decision Date2007-06-28
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SMS GLUCOSE CONTROL, MODEL 2120059 is the device name listed in this FDA 510(k) record. The listed applicant is Specialty Medical Supplies. It received FDA 510(k) clearance on 2007-06-28 under 510(k) number K071433. 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 SMS GLUCOSE CONTROL, MODEL 2120059?

SMS GLUCOSE CONTROL, MODEL 2120059 is a medical device that received FDA 510(k) clearance on 2007-06-28. The listed applicant is Specialty Medical Supplies. The 510(k) number is K071433.

When did SMS GLUCOSE CONTROL, MODEL 2120059 receive FDA 510(k) clearance?

SMS GLUCOSE CONTROL, MODEL 2120059 received FDA 510(k) clearance on 2007-06-28, under 510(k) number K071433.

Who is the listed applicant for SMS GLUCOSE CONTROL, MODEL 2120059?

The FDA 510(k) record lists Specialty Medical Supplies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SMS GLUCOSE CONTROL, MODEL 2120059?

The FDA product code for SMS GLUCOSE CONTROL, MODEL 2120059 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

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.

↑