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)

ANEMOMETER, NASAL, EXETER

K-Number: K781218 · 1978-07-27

ApplicantMedika Corp.
Decision Date1978-07-27
Product CodeETL
DecisionSubstantially Equivalent

Device Summary

ANEMOMETER, NASAL, EXETER is the device name listed in this FDA 510(k) record. The listed applicant is Medika Corp.. It received FDA 510(k) clearance on 1978-07-27 under 510(k) number K781218. The device is classified under product code ETL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANEMOMETER, NASAL, EXETER?

ANEMOMETER, NASAL, EXETER is a medical device that received FDA 510(k) clearance on 1978-07-27. The listed applicant is Medika Corp.. The 510(k) number is K781218.

When did ANEMOMETER, NASAL, EXETER receive FDA 510(k) clearance?

ANEMOMETER, NASAL, EXETER received FDA 510(k) clearance on 1978-07-27, under 510(k) number K781218.

Who is the listed applicant for ANEMOMETER, NASAL, EXETER?

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

What is the FDA product code for ANEMOMETER, NASAL, EXETER?

The FDA product code for ANEMOMETER, NASAL, EXETER is ETL.

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: ETL)

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.

K791937ATMOS ENT PATIENT CHAIR #1Jedmed Instrument Co.K791938ATMOS ENT PATIENT CHAIR #5Jedmed Instrument Co.K772193NASSAL PRESSURE/FLOW RECORDERAdco Labs.

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.

↑