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FDA 510(k)

KODAK DENTAL BARRIER PAC

K-Number: K884827 · 1989-01-30

Decision Date1989-01-30
Product CodeIWZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KODAK DENTAL BARRIER PAC is the device name listed in this FDA 510(k) record. The listed applicant is Eastman Kodak Company. It received FDA 510(k) clearance on 1989-01-30 under 510(k) number K884827. The device is classified under product code IWZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KODAK DENTAL BARRIER PAC?

KODAK DENTAL BARRIER PAC is a medical device that received FDA 510(k) clearance on 1989-01-30. The listed applicant is Eastman Kodak Company. The 510(k) number is K884827.

When did KODAK DENTAL BARRIER PAC receive FDA 510(k) clearance?

KODAK DENTAL BARRIER PAC received FDA 510(k) clearance on 1989-01-30, under 510(k) number K884827.

Who is the listed applicant for KODAK DENTAL BARRIER PAC?

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

What is the FDA product code for KODAK DENTAL BARRIER PAC?

The FDA product code for KODAK DENTAL BARRIER PAC is IWZ.

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 Eastman Kodak Company 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 238 devices →

Related Devices (Code: IWZ)

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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