MICRO-BOND HI-LIFE PROCELAIN & VIVERE
K-Number: K802235 · 1980-09-26
Advertisement
Device Summary
Frequently Asked Questions
What is the MICRO-BOND HI-LIFE PROCELAIN & VIVERE?
MICRO-BOND HI-LIFE PROCELAIN & VIVERE is a medical device that received FDA 510(k) clearance on 1980-09-26. The listed applicant is Howmedica Corp.. The 510(k) number is K802235.
When did MICRO-BOND HI-LIFE PROCELAIN & VIVERE receive FDA 510(k) clearance?
MICRO-BOND HI-LIFE PROCELAIN & VIVERE received FDA 510(k) clearance on 1980-09-26, under 510(k) number K802235.
Who is the listed applicant for MICRO-BOND HI-LIFE PROCELAIN & VIVERE?
The FDA 510(k) record lists Howmedica Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICRO-BOND HI-LIFE PROCELAIN & VIVERE?
The FDA product code for MICRO-BOND HI-LIFE PROCELAIN & VIVERE is EIH.
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 Howmedica 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: EIH)
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.
Advertisement