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FDA 510(k)

BILSOM PROPP

K-Number: K791608 · 1979-10-10

ApplicantBilson International, Inc.
Decision Date1979-10-10
Product CodeEWD
DecisionSubstantially Equivalent

Device Summary

BILSOM PROPP is the device name listed in this FDA 510(k) record. The listed applicant is Bilson International, Inc.. It received FDA 510(k) clearance on 1979-10-10 under 510(k) number K791608. The device is classified under product code EWD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BILSOM PROPP?

BILSOM PROPP is a medical device that received FDA 510(k) clearance on 1979-10-10. The listed applicant is Bilson International, Inc.. The 510(k) number is K791608.

When did BILSOM PROPP receive FDA 510(k) clearance?

BILSOM PROPP received FDA 510(k) clearance on 1979-10-10, under 510(k) number K791608.

Who is the listed applicant for BILSOM PROPP?

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

What is the FDA product code for BILSOM PROPP?

The FDA product code for BILSOM PROPP is EWD.

Related Clinical Trials

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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