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FDA 510(k)

DISPOSA-SHIELD(TM) INFECTION CONTROL BARRIER

K-Number: K900093 · 1990-04-06

Decision Date1990-04-06
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DISPOSA-SHIELD(TM) INFECTION CONTROL BARRIER is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1990-04-06 under 510(k) number K900093. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSA-SHIELD(TM) INFECTION CONTROL BARRIER?

DISPOSA-SHIELD(TM) INFECTION CONTROL BARRIER is a medical device that received FDA 510(k) clearance on 1990-04-06. The listed applicant is Dentsply Intl.. The 510(k) number is K900093.

When did DISPOSA-SHIELD(TM) INFECTION CONTROL BARRIER receive FDA 510(k) clearance?

DISPOSA-SHIELD(TM) INFECTION CONTROL BARRIER received FDA 510(k) clearance on 1990-04-06, under 510(k) number K900093.

Who is the listed applicant for DISPOSA-SHIELD(TM) INFECTION CONTROL BARRIER?

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

What is the FDA product code for DISPOSA-SHIELD(TM) INFECTION CONTROL BARRIER?

The FDA product code for DISPOSA-SHIELD(TM) INFECTION CONTROL BARRIER is EFB.

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 Dentsply Intl. 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 279 devices →

Related Devices (Code: EFB)

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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