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FDA 510(k)

PANAVIA EX, A DENTAL ADHESIVE

K-Number: K855211 · 1986-03-13

ApplicantKuraray Co.
Decision Date1986-03-13
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PANAVIA EX, A DENTAL ADHESIVE is the device name listed in this FDA 510(k) record. The listed applicant is Kuraray Co.. It received FDA 510(k) clearance on 1986-03-13 under 510(k) number K855211. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PANAVIA EX, A DENTAL ADHESIVE?

PANAVIA EX, A DENTAL ADHESIVE is a medical device that received FDA 510(k) clearance on 1986-03-13. The listed applicant is Kuraray Co.. The 510(k) number is K855211.

When did PANAVIA EX, A DENTAL ADHESIVE receive FDA 510(k) clearance?

PANAVIA EX, A DENTAL ADHESIVE received FDA 510(k) clearance on 1986-03-13, under 510(k) number K855211.

Who is the listed applicant for PANAVIA EX, A DENTAL ADHESIVE?

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

What is the FDA product code for PANAVIA EX, A DENTAL ADHESIVE?

The FDA product code for PANAVIA EX, A DENTAL ADHESIVE is EMA.

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 Kuraray Co. 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.

View all 25 devices →

Related Devices (Code: EMA)

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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