FDA 510(k)

ELECTROSURGICAL LATERAL RELEASE PROBE MOD ALR-100

K-Number: K852683 · 1985-08-12

Decision Date1985-08-12

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

ELECTROSURGICAL LATERAL RELEASE PROBE MOD ALR-100 is the device name listed in this FDA 510(k) record. The listed applicant is American Bentley. It received FDA 510(k) clearance on 1985-08-12 under 510(k) number K852683. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROSURGICAL LATERAL RELEASE PROBE MOD ALR-100?

ELECTROSURGICAL LATERAL RELEASE PROBE MOD ALR-100 is a medical device that received FDA 510(k) clearance on 1985-08-12. The listed applicant is American Bentley. The 510(k) number is K852683.

When did ELECTROSURGICAL LATERAL RELEASE PROBE MOD ALR-100 receive FDA 510(k) clearance?

ELECTROSURGICAL LATERAL RELEASE PROBE MOD ALR-100 received FDA 510(k) clearance on 1985-08-12, under 510(k) number K852683.

Who is the listed applicant for ELECTROSURGICAL LATERAL RELEASE PROBE MOD ALR-100?

The FDA 510(k) record lists American Bentley as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTROSURGICAL LATERAL RELEASE PROBE MOD ALR-100?

The FDA product code for ELECTROSURGICAL LATERAL RELEASE PROBE MOD ALR-100 is GEI.

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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.