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FDA 510(k)

ESPE NIMETIC-GRIP

K-Number: K844844 · 1986-02-13

ApplicantEspe GmbH (Us)
Decision Date1986-02-13
Product CodeDYH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ESPE NIMETIC-GRIP 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 1986-02-13 under 510(k) number K844844. The device is classified under product code DYH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESPE NIMETIC-GRIP?

ESPE NIMETIC-GRIP is a medical device that received FDA 510(k) clearance on 1986-02-13. The listed applicant is Espe GmbH (Us). The 510(k) number is K844844.

When did ESPE NIMETIC-GRIP receive FDA 510(k) clearance?

ESPE NIMETIC-GRIP received FDA 510(k) clearance on 1986-02-13, under 510(k) number K844844.

Who is the listed applicant for ESPE NIMETIC-GRIP?

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 ESPE NIMETIC-GRIP?

The FDA product code for ESPE NIMETIC-GRIP is DYH.

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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 APLICAPK915005PHOTAC-BOND APLICAP, MODIFICATIONK913966SONO(R) -CEMK913857ROCATEC(R) -PLUSK913965ESPE(R) -SILK905604VISIO-GEM ART-SYSTEM

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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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