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FDA 510(k)

BOWIE-DICK MINI PAK, MODEL BD 115

K-Number: K024293 · 2003-08-11

ApplicantSteritec Products, Inc.
Decision Date2003-08-11
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BOWIE-DICK MINI PAK, MODEL BD 115 is the device name listed in this FDA 510(k) record. The listed applicant is Steritec Products, Inc.. It received FDA 510(k) clearance on 2003-08-11 under 510(k) number K024293. 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 BOWIE-DICK MINI PAK, MODEL BD 115?

BOWIE-DICK MINI PAK, MODEL BD 115 is a medical device that received FDA 510(k) clearance on 2003-08-11. The listed applicant is Steritec Products, Inc.. The 510(k) number is K024293.

When did BOWIE-DICK MINI PAK, MODEL BD 115 receive FDA 510(k) clearance?

BOWIE-DICK MINI PAK, MODEL BD 115 received FDA 510(k) clearance on 2003-08-11, under 510(k) number K024293.

Who is the listed applicant for BOWIE-DICK MINI PAK, MODEL BD 115?

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

What is the FDA product code for BOWIE-DICK MINI PAK, MODEL BD 115?

The FDA product code for BOWIE-DICK MINI PAK, MODEL BD 115 is JOJ.

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Other records listing Steritec Products, Inc. as applicant

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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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