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FDA 510(k)

STAGE- 1 TEMPORARY/HEALING CAP, MODEL 42021-42026

K-Number: K053643 · 2006-01-23

ApplicantLifecore Biomedical, Inc.
Decision Date2006-01-23
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STAGE- 1 TEMPORARY/HEALING CAP, MODEL 42021-42026 is the device name listed in this FDA 510(k) record. The listed applicant is Lifecore Biomedical, Inc.. It received FDA 510(k) clearance on 2006-01-23 under 510(k) number K053643. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAGE- 1 TEMPORARY/HEALING CAP, MODEL 42021-42026?

STAGE- 1 TEMPORARY/HEALING CAP, MODEL 42021-42026 is a medical device that received FDA 510(k) clearance on 2006-01-23. The listed applicant is Lifecore Biomedical, Inc.. The 510(k) number is K053643.

When did STAGE- 1 TEMPORARY/HEALING CAP, MODEL 42021-42026 receive FDA 510(k) clearance?

STAGE- 1 TEMPORARY/HEALING CAP, MODEL 42021-42026 received FDA 510(k) clearance on 2006-01-23, under 510(k) number K053643.

Who is the listed applicant for STAGE- 1 TEMPORARY/HEALING CAP, MODEL 42021-42026?

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

What is the FDA product code for STAGE- 1 TEMPORARY/HEALING CAP, MODEL 42021-42026?

The FDA product code for STAGE- 1 TEMPORARY/HEALING CAP, MODEL 42021-42026 is NHA.

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Other records listing Lifecore Biomedical, Inc. as applicant

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Related Devices (Code: NHA)

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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