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FDA 510(k)

TITANIUM PROBES

K-Number: K852415 · 1985-08-02

ApplicantL.A.S.E.R., Inc.
Decision Date1985-08-02
Product CodeGAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TITANIUM PROBES is the device name listed in this FDA 510(k) record. The listed applicant is L.A.S.E.R., Inc.. It received FDA 510(k) clearance on 1985-08-02 under 510(k) number K852415. The device is classified under product code GAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TITANIUM PROBES?

TITANIUM PROBES is a medical device that received FDA 510(k) clearance on 1985-08-02. The listed applicant is L.A.S.E.R., Inc.. The 510(k) number is K852415.

When did TITANIUM PROBES receive FDA 510(k) clearance?

TITANIUM PROBES received FDA 510(k) clearance on 1985-08-02, under 510(k) number K852415.

Who is the listed applicant for TITANIUM PROBES?

The FDA 510(k) record lists L.A.S.E.R., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TITANIUM PROBES?

The FDA product code for TITANIUM PROBES is GAD.

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Other records listing L.A.S.E.R., Inc. as applicant

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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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