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)

MODEL 3D3 OSMOMETER

K-Number: K925970 · 1993-07-09

ApplicantAdvanced Instruments, Inc.
Decision Date1993-07-09
Product CodeJJM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MODEL 3D3 OSMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Instruments, Inc.. It received FDA 510(k) clearance on 1993-07-09 under 510(k) number K925970. The device is classified under product code JJM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 3D3 OSMOMETER?

MODEL 3D3 OSMOMETER is a medical device that received FDA 510(k) clearance on 1993-07-09. The listed applicant is Advanced Instruments, Inc.. The 510(k) number is K925970.

When did MODEL 3D3 OSMOMETER receive FDA 510(k) clearance?

MODEL 3D3 OSMOMETER received FDA 510(k) clearance on 1993-07-09, under 510(k) number K925970.

Who is the listed applicant for MODEL 3D3 OSMOMETER?

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

What is the FDA product code for MODEL 3D3 OSMOMETER?

The FDA product code for MODEL 3D3 OSMOMETER is JJM.

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 Advanced Instruments, 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.

K152776Glocyte Automated Cell Counter SystemK120631PATIENT MONITORK112465VITAL SIGNS MONITORK965036THE ADVANCED OSMOMETER (3900)K962056ADVANCED MICRO-OSMOMETER MODEL 3300K930526INTERMITTENT COMPRESSION SYSTEM MODEL 5000

View all 16 devices →

Related Devices (Code: JJM)

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.

K965036THE ADVANCED OSMOMETER (3900)Advanced Instruments, Inc.K962056ADVANCED MICRO-OSMOMETER MODEL 3300Advanced Instruments, Inc.K911092OSMOMETER MODEL 2400Advanced Instruments, Inc.K873642OSMOMETER MODEL 110Advanced Instruments, Inc.K843997AO-10 AUTOMATED OSMOMETERbioMerieux, Inc.K842750OSMOTIC PRESSURE AUTO & STAT OM-6010Kyoto Diagnostics, 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.

↑