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FDA 510(k)

MODIFIED ESCHMANN DILATATION CATHETER

K-Number: K864637 · 1987-01-06

ApplicantEschmann Bros. & Walsh , Ltd.
Decision Date1987-01-06
Product Code
DecisionSubstantially Equivalent

Device Summary

MODIFIED ESCHMANN DILATATION CATHETER 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 1987-01-06 under 510(k) number K864637. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED ESCHMANN DILATATION CATHETER?

MODIFIED ESCHMANN DILATATION CATHETER is a medical device that received FDA 510(k) clearance on 1987-01-06. The listed applicant is Eschmann Bros. & Walsh , Ltd.. The 510(k) number is K864637.

When did MODIFIED ESCHMANN DILATATION CATHETER receive FDA 510(k) clearance?

MODIFIED ESCHMANN DILATATION CATHETER received FDA 510(k) clearance on 1987-01-06, under 510(k) number K864637.

Who is the listed applicant for MODIFIED ESCHMANN DILATATION CATHETER?

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

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.

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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.

K852935ESCHMANN ELECTROSURGICAL UNIT, MODEL TD411K781863DEVICE, FEMALE INCONTINENCE

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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