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FDA 510(k)

IONOSIT BOND

K-Number: K991172 · 1999-05-17

ApplicantDmg Chemisch Pharmazeutische Fabrik GmbH
Decision Date1999-05-17
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IONOSIT BOND is the device name listed in this FDA 510(k) record. The listed applicant is Dmg Chemisch Pharmazeutische Fabrik GmbH. It received FDA 510(k) clearance on 1999-05-17 under 510(k) number K991172. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IONOSIT BOND?

IONOSIT BOND is a medical device that received FDA 510(k) clearance on 1999-05-17. The listed applicant is Dmg Chemisch Pharmazeutische Fabrik GmbH. The 510(k) number is K991172.

When did IONOSIT BOND receive FDA 510(k) clearance?

IONOSIT BOND received FDA 510(k) clearance on 1999-05-17, under 510(k) number K991172.

Who is the listed applicant for IONOSIT BOND?

The FDA 510(k) record lists Dmg Chemisch Pharmazeutische Fabrik GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IONOSIT BOND?

The FDA product code for IONOSIT BOND is EMA.

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Other records listing Dmg Chemisch Pharmazeutische Fabrik GmbH as applicant

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Related Devices (Code: EMA)

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

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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