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FDA 510(k)

DUAL CHAMBER MIXING BAG

K-Number: K926123 · 1993-09-03

ApplicantSecure Medical, Inc.
Decision Date1993-09-03
Product CodeKPE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DUAL CHAMBER MIXING BAG is the device name listed in this FDA 510(k) record. The listed applicant is Secure Medical, Inc.. It received FDA 510(k) clearance on 1993-09-03 under 510(k) number K926123. The device is classified under product code KPE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUAL CHAMBER MIXING BAG?

DUAL CHAMBER MIXING BAG is a medical device that received FDA 510(k) clearance on 1993-09-03. The listed applicant is Secure Medical, Inc.. The 510(k) number is K926123.

When did DUAL CHAMBER MIXING BAG receive FDA 510(k) clearance?

DUAL CHAMBER MIXING BAG received FDA 510(k) clearance on 1993-09-03, under 510(k) number K926123.

Who is the listed applicant for DUAL CHAMBER MIXING BAG?

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

What is the FDA product code for DUAL CHAMBER MIXING BAG?

The FDA product code for DUAL CHAMBER MIXING BAG is KPE.

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Related Devices (Code: KPE)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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