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FDA 510(k)

RELIANCE CI PROCESS INDICATOR

K-Number: K063285 · 2007-01-12

ApplicantAlbert Browne , Ltd.
Decision Date2007-01-12
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RELIANCE CI PROCESS INDICATOR 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 2007-01-12 under 510(k) number K063285. 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 RELIANCE CI PROCESS INDICATOR?

RELIANCE CI PROCESS INDICATOR is a medical device that received FDA 510(k) clearance on 2007-01-12. The listed applicant is Albert Browne , Ltd.. The 510(k) number is K063285.

When did RELIANCE CI PROCESS INDICATOR receive FDA 510(k) clearance?

RELIANCE CI PROCESS INDICATOR received FDA 510(k) clearance on 2007-01-12, under 510(k) number K063285.

Who is the listed applicant for RELIANCE CI PROCESS INDICATOR?

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 RELIANCE CI PROCESS INDICATOR?

The FDA product code for RELIANCE CI PROCESS INDICATOR 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.

K061738ALBERT BROWNE LTD. VERIFY STEAM AND EO LOAD RECORD CARDK053479VERIFY DRY HEAT LABELK060066VERIFY 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)

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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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