PRESCOTT'S SURGICAL SPEAR
K-Number: K003842 · 2001-04-13
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Device Summary
Frequently Asked Questions
What is the PRESCOTT'S SURGICAL SPEAR?
PRESCOTT'S SURGICAL SPEAR is a medical device that received FDA 510(k) clearance on 2001-04-13. The listed applicant is Prescott'S, Inc.. The 510(k) number is K003842.
When did PRESCOTT'S SURGICAL SPEAR receive FDA 510(k) clearance?
PRESCOTT'S SURGICAL SPEAR received FDA 510(k) clearance on 2001-04-13, under 510(k) number K003842.
Who is the listed applicant for PRESCOTT'S SURGICAL SPEAR?
The FDA 510(k) record lists Prescott'S, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRESCOTT'S SURGICAL SPEAR?
The FDA product code for PRESCOTT'S SURGICAL SPEAR 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 Prescott'S, 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: 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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