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FDA 510(k)

PALAMED G

K-Number: K050855 · 2005-07-07

ApplicantHeraeus Kulzer,GmbH
Decision Date2005-07-07
Product CodeLOD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PALAMED G is the device name listed in this FDA 510(k) record. The listed applicant is Heraeus Kulzer,GmbH. It received FDA 510(k) clearance on 2005-07-07 under 510(k) number K050855. The device is classified under product code LOD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PALAMED G?

PALAMED G is a medical device that received FDA 510(k) clearance on 2005-07-07. The listed applicant is Heraeus Kulzer,GmbH. The 510(k) number is K050855.

When did PALAMED G receive FDA 510(k) clearance?

PALAMED G received FDA 510(k) clearance on 2005-07-07, under 510(k) number K050855.

Who is the listed applicant for PALAMED G?

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

What is the FDA product code for PALAMED G?

The FDA product code for PALAMED G is LOD.

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Other records listing Heraeus Kulzer,GmbH 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.

K083652IBOND TOTAL ETCHK080338CUTTERSIL ACTIVATOR UNIVERSAL PLUSK073554NEUNK062515RETENTION FLOW OPAQUEK050085OSTEOPAL VK050854PALACOS LV+G

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Related Devices (Code: LOD)

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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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