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FDA 510(k)

SPATULA, DENTAL, CEMENT

K-Number: K871818 · 1987-07-02

Decision Date1987-07-02
Product CodeEJB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SPATULA, DENTAL, CEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Military Engineering, Inc.. It received FDA 510(k) clearance on 1987-07-02 under 510(k) number K871818. The device is classified under product code EJB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPATULA, DENTAL, CEMENT?

SPATULA, DENTAL, CEMENT is a medical device that received FDA 510(k) clearance on 1987-07-02. The listed applicant is Military Engineering, Inc.. The 510(k) number is K871818.

When did SPATULA, DENTAL, CEMENT receive FDA 510(k) clearance?

SPATULA, DENTAL, CEMENT received FDA 510(k) clearance on 1987-07-02, under 510(k) number K871818.

Who is the listed applicant for SPATULA, DENTAL, CEMENT?

The FDA 510(k) record lists Military Engineering, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPATULA, DENTAL, CEMENT?

The FDA product code for SPATULA, DENTAL, CEMENT is EJB.

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 Military Engineering, Inc. 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 17 devices →

Related Devices (Code: EJB)

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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