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FDA 510(k)

VITAPATCH PIN PROTECTION DEVICE FOR PERCUT. PINS

K-Number: K872538 · 1987-07-10

Decision Date1987-07-10
Product CodeJEC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VITAPATCH PIN PROTECTION DEVICE FOR PERCUT. PINS is the device name listed in this FDA 510(k) record. The listed applicant is Vitaphore Corp.. It received FDA 510(k) clearance on 1987-07-10 under 510(k) number K872538. The device is classified under product code JEC. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 13 devices →

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

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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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