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FDA 510(k)

TOOTH SLOOTH

K-Number: K833338 · 1983-11-25

ApplicantJoel Lander D.D.S.
Decision Date1983-11-25
Product CodeEJB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TOOTH SLOOTH is the device name listed in this FDA 510(k) record. The listed applicant is Joel Lander D.D.S.. It received FDA 510(k) clearance on 1983-11-25 under 510(k) number K833338. The device is classified under product code EJB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOOTH SLOOTH?

TOOTH SLOOTH is a medical device that received FDA 510(k) clearance on 1983-11-25. The listed applicant is Joel Lander D.D.S.. The 510(k) number is K833338.

When did TOOTH SLOOTH receive FDA 510(k) clearance?

TOOTH SLOOTH received FDA 510(k) clearance on 1983-11-25, under 510(k) number K833338.

Who is the listed applicant for TOOTH SLOOTH?

The FDA 510(k) record lists Joel Lander D.D.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TOOTH SLOOTH?

The FDA product code for TOOTH SLOOTH is EJB.

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Related Devices (Code: EJB)

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.

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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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