EXA BITE REGISTRATION MATERIAL
K-Number: K933206 · 1993-09-29
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Device Summary
Frequently Asked Questions
What is the EXA BITE REGISTRATION MATERIAL?
EXA BITE REGISTRATION MATERIAL is a medical device that received FDA 510(k) clearance on 1993-09-29. The listed applicant is GC America, Inc.. The 510(k) number is K933206.
When did EXA BITE REGISTRATION MATERIAL receive FDA 510(k) clearance?
EXA BITE REGISTRATION MATERIAL received FDA 510(k) clearance on 1993-09-29, under 510(k) number K933206.
Who is the listed applicant for EXA BITE REGISTRATION MATERIAL?
The FDA 510(k) record lists GC America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EXA BITE REGISTRATION MATERIAL?
The FDA product code for EXA BITE REGISTRATION MATERIAL is ELW.
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 GC America, 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: ELW)
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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