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FDA 510(k)

DEVICE, FEMALE INCONTINENCE

K-Number: K781863 · 1978-11-06

ApplicantEschmann Bros. & Walsh , Ltd.
Decision Date1978-11-06
Product CodeHHW
Advisory CommitteeOB
DecisionUnknown

Device Summary

DEVICE, FEMALE INCONTINENCE 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 1978-11-06 under 510(k) number K781863. The device is classified under product code HHW. It was reviewed by the OB advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the DEVICE, FEMALE INCONTINENCE?

DEVICE, FEMALE INCONTINENCE is a medical device that received FDA 510(k) clearance on 1978-11-06. The listed applicant is Eschmann Bros. & Walsh , Ltd.. The 510(k) number is K781863.

When did DEVICE, FEMALE INCONTINENCE receive FDA 510(k) clearance?

DEVICE, FEMALE INCONTINENCE received FDA 510(k) clearance on 1978-11-06, under 510(k) number K781863.

Who is the listed applicant for DEVICE, FEMALE INCONTINENCE?

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 DEVICE, FEMALE INCONTINENCE?

The FDA product code for DEVICE, FEMALE INCONTINENCE is HHW.

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.

K864637MODIFIED ESCHMANN DILATATION CATHETERK852935ESCHMANN ELECTROSURGICAL UNIT, MODEL TD411

Related Devices (Code: HHW)

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

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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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