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FDA 510(k)

PERFECT CHOICE

K-Number: K884245 · 1989-01-04

ApplicantChallenge Products, Inc.
Decision Date1989-01-04
Product CodeEJK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PERFECT CHOICE is the device name listed in this FDA 510(k) record. The listed applicant is Challenge Products, Inc.. It received FDA 510(k) clearance on 1989-01-04 under 510(k) number K884245. The device is classified under product code EJK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERFECT CHOICE?

PERFECT CHOICE is a medical device that received FDA 510(k) clearance on 1989-01-04. The listed applicant is Challenge Products, Inc.. The 510(k) number is K884245.

When did PERFECT CHOICE receive FDA 510(k) clearance?

PERFECT CHOICE received FDA 510(k) clearance on 1989-01-04, under 510(k) number K884245.

Who is the listed applicant for PERFECT CHOICE?

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

What is the FDA product code for PERFECT CHOICE?

The FDA product code for PERFECT CHOICE is EJK.

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.

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Other records listing Challenge Products, Inc. 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.

K962370PERFECT CHOICE PROPHY PASTE WITH 10% CARBAMIDE PEROXIDEK940496PROPHY PASTEK853248CHALLENGER SUNRISE

Related Devices (Code: EJK)

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.

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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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