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FDA 510(k)

MODEL 322 CLINICAL AUDIOMETER

K-Number: K930203 · 1993-07-08

ApplicantVirtual Corp.
Decision Date1993-07-08
Product CodeEWD
DecisionSubstantially Equivalent

Device Summary

MODEL 322 CLINICAL AUDIOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Virtual Corp.. It received FDA 510(k) clearance on 1993-07-08 under 510(k) number K930203. The device is classified under product code EWD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 322 CLINICAL AUDIOMETER?

MODEL 322 CLINICAL AUDIOMETER is a medical device that received FDA 510(k) clearance on 1993-07-08. The listed applicant is Virtual Corp.. The 510(k) number is K930203.

When did MODEL 322 CLINICAL AUDIOMETER receive FDA 510(k) clearance?

MODEL 322 CLINICAL AUDIOMETER received FDA 510(k) clearance on 1993-07-08, under 510(k) number K930203.

Who is the listed applicant for MODEL 322 CLINICAL AUDIOMETER?

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

What is the FDA product code for MODEL 322 CLINICAL AUDIOMETER?

The FDA product code for MODEL 322 CLINICAL AUDIOMETER is EWD.

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 Virtual 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.

K960500THE VIRTUAL M-332K934715MODEL 222 CLINICAL AUDIOMETERK926574MODEL 330 SCREENING AUDIO METER, MODIFIEDK911689MODEL 330 SCREENING AUDIOMETERK896301MODEL 340 PROBE MIC SYSTEMK895443MODEL 210 IMPEDANCE SYSTEM

View all 9 devices →

Related Devices (Code: EWD)

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.

K020296ADULT SILICONE EAR PLUGS, MODELS # 68053, 68057Apothecary Products, Inc.K972923SUPER SILIPLUGS EAR PLUGSInterview Medical Technology Corp.K971517SILICONE PUTTY EAR PLUGSBentec Medical, Inc.K962292HEARSAVEREmtech LaboratoriesK960500THE VIRTUAL M-332Virtual Corp.K945376DOC'S PROPLUGS EAR PLUGSDoc'S Proplugs, 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.

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