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FDA 510(k)

DENTAL FLOSS PICK

K-Number: K882828 · 1988-08-12

ApplicantBik Pik
Decision Date1988-08-12
Product CodeJES
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL FLOSS PICK is the device name listed in this FDA 510(k) record. The listed applicant is Bik Pik. It received FDA 510(k) clearance on 1988-08-12 under 510(k) number K882828. The device is classified under product code JES. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTAL FLOSS PICK?

DENTAL FLOSS PICK is a medical device that received FDA 510(k) clearance on 1988-08-12. The listed applicant is Bik Pik. The 510(k) number is K882828.

When did DENTAL FLOSS PICK receive FDA 510(k) clearance?

DENTAL FLOSS PICK received FDA 510(k) clearance on 1988-08-12, under 510(k) number K882828.

Who is the listed applicant for DENTAL FLOSS PICK?

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

What is the FDA product code for DENTAL FLOSS PICK?

The FDA product code for DENTAL FLOSS PICK is JES.

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.

Related Devices (Code: JES)

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.

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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