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FDA 510(k)

CURRETTES, ALVEOLAR (MOLT AND MILLER)

K-Number: K872091 · 1987-07-31

Decision Date1987-07-31
Product CodeEMS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CURRETTES, ALVEOLAR (MOLT AND MILLER) 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 1987-07-31 under 510(k) number K872091. The device is classified under product code EMS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURRETTES, ALVEOLAR (MOLT AND MILLER)?

CURRETTES, ALVEOLAR (MOLT AND MILLER) is a medical device that received FDA 510(k) clearance on 1987-07-31. The listed applicant is Military Engineering, Inc.. The 510(k) number is K872091.

When did CURRETTES, ALVEOLAR (MOLT AND MILLER) receive FDA 510(k) clearance?

CURRETTES, ALVEOLAR (MOLT AND MILLER) received FDA 510(k) clearance on 1987-07-31, under 510(k) number K872091.

Who is the listed applicant for CURRETTES, ALVEOLAR (MOLT AND MILLER)?

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 CURRETTES, ALVEOLAR (MOLT AND MILLER)?

The FDA product code for CURRETTES, ALVEOLAR (MOLT AND MILLER) is EMS.

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: EMS)

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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