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FDA 510(k)

STERI-PAK LF BOWIE-DICK TEST PACK

K-Number: K990246 · 1999-06-10

ApplicantSteritec Products Mfg Co, Inc.
Decision Date1999-06-10
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERI-PAK LF BOWIE-DICK TEST PACK is the device name listed in this FDA 510(k) record. The listed applicant is Steritec Products Mfg Co, Inc.. It received FDA 510(k) clearance on 1999-06-10 under 510(k) number K990246. 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 STERI-PAK LF BOWIE-DICK TEST PACK?

STERI-PAK LF BOWIE-DICK TEST PACK is a medical device that received FDA 510(k) clearance on 1999-06-10. The listed applicant is Steritec Products Mfg Co, Inc.. The 510(k) number is K990246.

When did STERI-PAK LF BOWIE-DICK TEST PACK receive FDA 510(k) clearance?

STERI-PAK LF BOWIE-DICK TEST PACK received FDA 510(k) clearance on 1999-06-10, under 510(k) number K990246.

Who is the listed applicant for STERI-PAK LF BOWIE-DICK TEST PACK?

The FDA 510(k) record lists Steritec Products Mfg Co, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERI-PAK LF BOWIE-DICK TEST PACK?

The FDA product code for STERI-PAK LF BOWIE-DICK TEST PACK is JOJ.

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Other records listing Steritec Products Mfg Co, Inc. as applicant

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K200252Getinge Assured MI Steam Migrating IntegratorK132372STERITEC GREEN CARD PACK BOWIE-DICK TESTK122945STERITEC GREEN CARD PACK BOWIE-DICK TEST MODEL BD 126K122555STERITEC LEAD FREE STERILIZATION PROCESS INDICATOR TAPEK111150STERITEC SMART-READ BIOLOGICAL TEST PACK WITH INSTANT READOUT INTEGRATORK103000SMART READ BIOLOGICAL TEST PACK

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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.

K2619923M™ Attest™ Steam Chemical Integrator (1243A, 1243B, 1243RE, 1243RES)Solventum US, LLCK260181LF Process Indicator Tape for Steam SterilizationIntertape Polymer GroupK251991SafeSecure Steam Sterilization Process Indicator (4012, 4013, 4014, 4016); SafeSecure Vaporized Hydrogen Peroxide Sterilization Process Indicator (4211, 4212, 4213)Shenzhen Safesecure Medical Infection Control Tech Co. , Ltd.K251035DISINTEK™ PA Test StripsSerim ResearchK251048Rapicide PA High-Level Disinfection Test Strip Model Ref # = ML02-0118STERIS CorporationK243876VERIFY STEAM Integrating IndicatorSTERIS Corporation

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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