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)

MED-A-CALL ASSIST DEVICE

K-Number: K890596 · 1989-03-14

ApplicantSilent Call Corp.
Decision Date1989-03-14
Product CodeIQA
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MED-A-CALL ASSIST DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Silent Call Corp.. It received FDA 510(k) clearance on 1989-03-14 under 510(k) number K890596. The device is classified under product code IQA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MED-A-CALL ASSIST DEVICE?

MED-A-CALL ASSIST DEVICE is a medical device that received FDA 510(k) clearance on 1989-03-14. The listed applicant is Silent Call Corp.. The 510(k) number is K890596.

When did MED-A-CALL ASSIST DEVICE receive FDA 510(k) clearance?

MED-A-CALL ASSIST DEVICE received FDA 510(k) clearance on 1989-03-14, under 510(k) number K890596.

Who is the listed applicant for MED-A-CALL ASSIST DEVICE?

The FDA 510(k) record lists Silent Call Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MED-A-CALL ASSIST DEVICE?

The FDA product code for MED-A-CALL ASSIST DEVICE is IQA.

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 Silent Call Corp. 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.

K890445PERSONAL ALERT ASSIST DEVICE

Related Devices (Code: IQA)

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.

K961306DELTATALKER WITH INFRAREDPrentke Romich Co.K953905IMPERIUMTeledyne Brown EngineeringK953937LIAISON COMPUTER ACCESS & ENVIRONMENTAL CONTROL SYSTEMApt Technology, Inc.K943244DEUCEApt Technology, Inc.K944585SCANNING DIRECTORPrentke Romich Co.K944345BEDSIDE BUTLERTrac 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.

↑