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FDA 510(k)

VERIFY DRY HEAT LABEL

K-Number: K053479 · 2006-07-18

ApplicantAlbert Browne , Ltd.
Decision Date2006-07-18
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VERIFY DRY HEAT LABEL is the device name listed in this FDA 510(k) record. The listed applicant is Albert Browne , Ltd.. It received FDA 510(k) clearance on 2006-07-18 under 510(k) number K053479. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERIFY DRY HEAT LABEL?

VERIFY DRY HEAT LABEL is a medical device that received FDA 510(k) clearance on 2006-07-18. The listed applicant is Albert Browne , Ltd.. The 510(k) number is K053479.

When did VERIFY DRY HEAT LABEL receive FDA 510(k) clearance?

VERIFY DRY HEAT LABEL received FDA 510(k) clearance on 2006-07-18, under 510(k) number K053479.

Who is the listed applicant for VERIFY DRY HEAT LABEL?

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

What is the FDA product code for VERIFY DRY HEAT LABEL?

The FDA product code for VERIFY DRY HEAT LABEL is JOJ.

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Other records listing Albert Browne , Ltd. 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.

K063285RELIANCE CI PROCESS INDICATORK061738ALBERT BROWNE LTD. VERIFY STEAM AND EO LOAD RECORD CARDK060066VERIFY 3-10 MIN FLASH INTEGRATORK060103ALBERT BROWNE LTD. VERIFY STEAM VALUE INDICATORSK051101VERIFY FLASH INTEGRATORK051056VERIFY SELF-CONTAINED BIOLOGICAL INDICATOR

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Related Devices (Code: JOJ)

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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