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FDA 510(k)

ESCHMANN ELECTROSURGICAL UNIT, MODEL TD411

K-Number: K852935 · 1985-10-10

ApplicantEschmann Bros. & Walsh , Ltd.
Decision Date1985-10-10
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ESCHMANN ELECTROSURGICAL UNIT, MODEL TD411 is the device name listed in this FDA 510(k) record. The listed applicant is Eschmann Bros. & Walsh , Ltd.. It received FDA 510(k) clearance on 1985-10-10 under 510(k) number K852935. 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 ESCHMANN ELECTROSURGICAL UNIT, MODEL TD411?

ESCHMANN ELECTROSURGICAL UNIT, MODEL TD411 is a medical device that received FDA 510(k) clearance on 1985-10-10. The listed applicant is Eschmann Bros. & Walsh , Ltd.. The 510(k) number is K852935.

When did ESCHMANN ELECTROSURGICAL UNIT, MODEL TD411 receive FDA 510(k) clearance?

ESCHMANN ELECTROSURGICAL UNIT, MODEL TD411 received FDA 510(k) clearance on 1985-10-10, under 510(k) number K852935.

Who is the listed applicant for ESCHMANN ELECTROSURGICAL UNIT, MODEL TD411?

The FDA 510(k) record lists Eschmann Bros. & Walsh , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ESCHMANN ELECTROSURGICAL UNIT, MODEL TD411?

The FDA product code for ESCHMANN ELECTROSURGICAL UNIT, MODEL TD411 is GEI.

Related Clinical Trials

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Other records listing Eschmann Bros. & Walsh , Ltd. as applicant

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.

K864637MODIFIED ESCHMANN DILATATION CATHETERK781863DEVICE, FEMALE INCONTINENCE

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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.

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