STERILIZED DENTAL BIT PACKAGING
K-Number: K873698 · 1987-12-03
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Device Summary
Frequently Asked Questions
What is the STERILIZED DENTAL BIT PACKAGING?
STERILIZED DENTAL BIT PACKAGING is a medical device that received FDA 510(k) clearance on 1987-12-03. The listed applicant is Florida Diamond Instruments Corp.. The 510(k) number is K873698.
When did STERILIZED DENTAL BIT PACKAGING receive FDA 510(k) clearance?
STERILIZED DENTAL BIT PACKAGING received FDA 510(k) clearance on 1987-12-03, under 510(k) number K873698.
Who is the listed applicant for STERILIZED DENTAL BIT PACKAGING?
The FDA 510(k) record lists Florida Diamond Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERILIZED DENTAL BIT PACKAGING?
The FDA product code for STERILIZED DENTAL BIT PACKAGING is EJL.
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.
Related Devices (Code: EJL)
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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