VITAPATCH PIN PROTECTION DEVICE FOR PERCUT. PINS
K-Number: K872538 · 1987-07-10
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Device Summary
Frequently Asked Questions
What is the VITAPATCH PIN PROTECTION DEVICE FOR PERCUT. PINS?
VITAPATCH PIN PROTECTION DEVICE FOR PERCUT. PINS is a medical device that received FDA 510(k) clearance on 1987-07-10. The listed applicant is Vitaphore Corp.. The 510(k) number is K872538.
When did VITAPATCH PIN PROTECTION DEVICE FOR PERCUT. PINS receive FDA 510(k) clearance?
VITAPATCH PIN PROTECTION DEVICE FOR PERCUT. PINS received FDA 510(k) clearance on 1987-07-10, under 510(k) number K872538.
Who is the listed applicant for VITAPATCH PIN PROTECTION DEVICE FOR PERCUT. PINS?
The FDA 510(k) record lists Vitaphore Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VITAPATCH PIN PROTECTION DEVICE FOR PERCUT. PINS?
The FDA product code for VITAPATCH PIN PROTECTION DEVICE FOR PERCUT. PINS is JEC.
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 Vitaphore 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: JEC)
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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