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 192 PRINTER

K-Number: K870538 · 1987-04-23

ApplicantAdvanced Medical Products, Inc.
Decision Date1987-04-23
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 192 PRINTER is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Medical Products, Inc.. It received FDA 510(k) clearance on 1987-04-23 under 510(k) number K870538. The device is classified under product code DSF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 192 PRINTER?

MODEL 192 PRINTER is a medical device that received FDA 510(k) clearance on 1987-04-23. The listed applicant is Advanced Medical Products, Inc.. The 510(k) number is K870538.

When did MODEL 192 PRINTER receive FDA 510(k) clearance?

MODEL 192 PRINTER received FDA 510(k) clearance on 1987-04-23, under 510(k) number K870538.

Who is the listed applicant for MODEL 192 PRINTER?

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

What is the FDA product code for MODEL 192 PRINTER?

The FDA product code for MODEL 192 PRINTER is DSF.

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 Medical Products, 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.

K000932ARACHNOPHLEBECTOMY NEEDLEK923995URODYNAMICS TUBING KITS #5161, #5150, #7170K921426ULTRA PCIK912925ULTRA PVDK915658SPECTRA ECGK896102MICRO FD 7000 AMBULATORY BLOOD PRESSURE MONITOR

View all 14 devices →

Related Devices (Code: DSF)

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.

K910871EDENTEC DIGITAL CHARTER MODEL 3710Edentec Corp.K912929DASH IVAstro-Med, Inc.K905856MODEL 556 MONITORGe Medical Systems Information TechnologiesK902586GRI LASERGRAPH(TM) ECG PAPERGri Medical Products, Inc.K902230COLORADO COLOR IMAGING RECORDERHoneywell, Inc.K901385GABRIEL MEDICAL CLS THERMAL RECORDERGabriel Medical, 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.

↑