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FDA 510(k)

DELTA PUNCTUM PLUG

K-Number: K050851 · 2005-08-19

ApplicantDelta Life Science, Inc.
Decision Date2005-08-19
Product CodeLZU
DecisionSubstantially Equivalent

Device Summary

DELTA PUNCTUM PLUG is the device name listed in this FDA 510(k) record. The listed applicant is Delta Life Science, Inc.. It received FDA 510(k) clearance on 2005-08-19 under 510(k) number K050851. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DELTA PUNCTUM PLUG?

DELTA PUNCTUM PLUG is a medical device that received FDA 510(k) clearance on 2005-08-19. The listed applicant is Delta Life Science, Inc.. The 510(k) number is K050851.

When did DELTA PUNCTUM PLUG receive FDA 510(k) clearance?

DELTA PUNCTUM PLUG received FDA 510(k) clearance on 2005-08-19, under 510(k) number K050851.

Who is the listed applicant for DELTA PUNCTUM PLUG?

The FDA 510(k) record lists Delta Life Science, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DELTA PUNCTUM PLUG?

The FDA product code for DELTA PUNCTUM PLUG is LZU.

Related Clinical Trials

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Related Devices (Code: LZU)

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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