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FDA 510(k)

PEMBUSH

K-Number: K942634 · 1994-09-02

ApplicantCrossroads Trading Co.
Decision Date1994-09-02
Product CodeJEQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PEMBUSH is the device name listed in this FDA 510(k) record. The listed applicant is Crossroads Trading Co.. It received FDA 510(k) clearance on 1994-09-02 under 510(k) number K942634. The device is classified under product code JEQ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEMBUSH?

PEMBUSH is a medical device that received FDA 510(k) clearance on 1994-09-02. The listed applicant is Crossroads Trading Co.. The 510(k) number is K942634.

When did PEMBUSH receive FDA 510(k) clearance?

PEMBUSH received FDA 510(k) clearance on 1994-09-02, under 510(k) number K942634.

Who is the listed applicant for PEMBUSH?

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

What is the FDA product code for PEMBUSH?

The FDA product code for PEMBUSH is JEQ.

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Related Devices (Code: JEQ)

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.

K200881Oral-B iO Test Drive Power Brush Trial Program KitThe Procter & Gamble CompanyK061351ORAL-B SONIC COMPLETEBraun GmbHK061199ORAL B PROFESSIONALCARE SERIES, ORAL B ADVANCEPOWER SERIESBraun GmbHK040416SONICARE ADVANCE TOOTHBRUSH, MODEL 4900Philips Oral Healthcare, Inc.K022900BUTLER GUM VARI-CLEAN POWER TOOTHBRUSHESJohn O. Butler Co.K012914SONICWAVE SONIC PLAQUE REMOVERHomedics, 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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