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FDA 510(k)

RANIR HI-TECHNOLOGY DENTAL FLOSS

K-Number: K955530 · 1995-12-28

Decision Date1995-12-28
Product CodeEFW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RANIR HI-TECHNOLOGY DENTAL FLOSS is the device name listed in this FDA 510(k) record. The listed applicant is Ranir/Dcp Corp.. It received FDA 510(k) clearance on 1995-12-28 under 510(k) number K955530. The device is classified under product code EFW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RANIR HI-TECHNOLOGY DENTAL FLOSS?

RANIR HI-TECHNOLOGY DENTAL FLOSS is a medical device that received FDA 510(k) clearance on 1995-12-28. The listed applicant is Ranir/Dcp Corp.. The 510(k) number is K955530.

When did RANIR HI-TECHNOLOGY DENTAL FLOSS receive FDA 510(k) clearance?

RANIR HI-TECHNOLOGY DENTAL FLOSS received FDA 510(k) clearance on 1995-12-28, under 510(k) number K955530.

Who is the listed applicant for RANIR HI-TECHNOLOGY DENTAL FLOSS?

The FDA 510(k) record lists Ranir/Dcp Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RANIR HI-TECHNOLOGY DENTAL FLOSS?

The FDA product code for RANIR HI-TECHNOLOGY DENTAL FLOSS is EFW.

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.

Other records listing Ranir/Dcp 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.

Related Devices (Code: EFW)

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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