CURRETTES, ALVEOLAR (MOLT AND MILLER)
K-Number: K872091 · 1987-07-31
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Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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