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FDA 510(k)

MFCD 1219, MFCD 1219 TS

K-Number: K052478 · 2005-09-28

ApplicantBarcoview
Decision Date2005-09-28
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MFCD 1219, MFCD 1219 TS is the device name listed in this FDA 510(k) record. The listed applicant is Barcoview. It received FDA 510(k) clearance on 2005-09-28 under 510(k) number K052478. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MFCD 1219, MFCD 1219 TS?

MFCD 1219, MFCD 1219 TS is a medical device that received FDA 510(k) clearance on 2005-09-28. The listed applicant is Barcoview. The 510(k) number is K052478.

When did MFCD 1219, MFCD 1219 TS receive FDA 510(k) clearance?

MFCD 1219, MFCD 1219 TS received FDA 510(k) clearance on 2005-09-28, under 510(k) number K052478.

Who is the listed applicant for MFCD 1219, MFCD 1219 TS?

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

What is the FDA product code for MFCD 1219, MFCD 1219 TS?

The FDA product code for MFCD 1219, MFCD 1219 TS is LLZ.

Other records listing Barcoview 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.

View all 17 devices →

Related Devices (Code: LLZ)

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.

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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