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FDA 510(k)

PERMADYNE ADHESIVE

K-Number: K875228 · 1988-03-09

ApplicantEspe GmbH (Us)
Decision Date1988-03-09
Product CodeEBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PERMADYNE ADHESIVE is the device name listed in this FDA 510(k) record. The listed applicant is Espe GmbH (Us). It received FDA 510(k) clearance on 1988-03-09 under 510(k) number K875228. The device is classified under product code EBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERMADYNE ADHESIVE?

PERMADYNE ADHESIVE is a medical device that received FDA 510(k) clearance on 1988-03-09. The listed applicant is Espe GmbH (Us). The 510(k) number is K875228.

When did PERMADYNE ADHESIVE receive FDA 510(k) clearance?

PERMADYNE ADHESIVE received FDA 510(k) clearance on 1988-03-09, under 510(k) number K875228.

Who is the listed applicant for PERMADYNE ADHESIVE?

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

What is the FDA product code for PERMADYNE ADHESIVE?

The FDA product code for PERMADYNE ADHESIVE is EBH.

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Other records listing Espe GmbH (Us) 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.

K925027PHOTAC-FIL APLICAPK913966SONO(R) -CEMK915005PHOTAC-BOND APLICAP, MODIFICATIONK913857ROCATEC(R) -PLUSK913965ESPE(R) -SILK905604VISIO-GEM ART-SYSTEM

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Related Devices (Code: EBH)

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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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