MICROSPEARS
K-Number: K896084 · 1989-11-02
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Device Summary
Frequently Asked Questions
What is the MICROSPEARS?
MICROSPEARS is a medical device that received FDA 510(k) clearance on 1989-11-02. The listed applicant is Sparta Surgical Corp.. The 510(k) number is K896084.
When did MICROSPEARS receive FDA 510(k) clearance?
MICROSPEARS received FDA 510(k) clearance on 1989-11-02, under 510(k) number K896084.
Who is the listed applicant for MICROSPEARS?
The FDA 510(k) record lists Sparta Surgical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICROSPEARS?
The FDA product code for MICROSPEARS is HOZ.
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 Sparta Surgical Corp. 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: HOZ)
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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