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FDA 510(k)

SUPER SILIPLUGS EAR PLUGS

K-Number: K972923 · 1997-10-27

ApplicantInterview Medical Technology Corp.
Decision Date1997-10-27
Product CodeEWD
DecisionSubstantially Equivalent

Device Summary

SUPER SILIPLUGS EAR PLUGS is the device name listed in this FDA 510(k) record. The listed applicant is Interview Medical Technology Corp.. It received FDA 510(k) clearance on 1997-10-27 under 510(k) number K972923. The device is classified under product code EWD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPER SILIPLUGS EAR PLUGS?

SUPER SILIPLUGS EAR PLUGS is a medical device that received FDA 510(k) clearance on 1997-10-27. The listed applicant is Interview Medical Technology Corp.. The 510(k) number is K972923.

When did SUPER SILIPLUGS EAR PLUGS receive FDA 510(k) clearance?

SUPER SILIPLUGS EAR PLUGS received FDA 510(k) clearance on 1997-10-27, under 510(k) number K972923.

Who is the listed applicant for SUPER SILIPLUGS EAR PLUGS?

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

What is the FDA product code for SUPER SILIPLUGS EAR PLUGS?

The FDA product code for SUPER SILIPLUGS EAR PLUGS 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 Interview Medical Technology 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.

K972922VYKER SILICONE EPISTAXIS CATHETER V-27030, VYKER SILICONE EPISTAXIS CATHETER KIT V-2703K

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.K971517SILICONE PUTTY EAR PLUGSBentec Medical, Inc.K962292HEARSAVEREmtech LaboratoriesK960500THE VIRTUAL M-332Virtual Corp.K945376DOC'S PROPLUGS EAR PLUGSDoc'S Proplugs, Inc.K930203MODEL 322 CLINICAL AUDIOMETERVirtual Corp.

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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