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FDA 510(k)

STERILIZED DENTAL BIT PACKAGING

K-Number: K873698 · 1987-12-03

Decision Date1987-12-03
Product CodeEJL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STERILIZED DENTAL BIT PACKAGING is the device name listed in this FDA 510(k) record. The listed applicant is Florida Diamond Instruments Corp.. It received FDA 510(k) clearance on 1987-12-03 under 510(k) number K873698. The device is classified under product code EJL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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

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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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