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FDA 510(k)

16 X 125 MM TEST TUBE, CATALOG

K-Number: K930397 · 1993-03-24

ApplicantProteins Intl., Inc.
Decision Date1993-03-24
Product CodeKIR
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

16 X 125 MM TEST TUBE, CATALOG is the device name listed in this FDA 510(k) record. The listed applicant is Proteins Intl., Inc.. It received FDA 510(k) clearance on 1993-03-24 under 510(k) number K930397. The device is classified under product code KIR. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 16 X 125 MM TEST TUBE, CATALOG?

16 X 125 MM TEST TUBE, CATALOG is a medical device that received FDA 510(k) clearance on 1993-03-24. The listed applicant is Proteins Intl., Inc.. The 510(k) number is K930397.

When did 16 X 125 MM TEST TUBE, CATALOG receive FDA 510(k) clearance?

16 X 125 MM TEST TUBE, CATALOG received FDA 510(k) clearance on 1993-03-24, under 510(k) number K930397.

Who is the listed applicant for 16 X 125 MM TEST TUBE, CATALOG?

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

What is the FDA product code for 16 X 125 MM TEST TUBE, CATALOG?

The FDA product code for 16 X 125 MM TEST TUBE, CATALOG is KIR.

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Other records listing Proteins Intl., Inc. 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.

K961755CYTOQUANT CHLAMYDIA TRANSPORT MEDIUMK961756CYTOQUANT VIRAL TRANSPORT MEDIUMK93039025 CM2, 75 CM2, 125 CM2 FLASK, CATALOG #03-291K93039216 X 125 MM TEST TUBE, CATALOG #01-111K93039425 CM2, 75 CM2, A50 CM2 FLASK, CATALOG #03-211K930393ONE DRAM SHELL VIAL, CATALOG #02-261

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Related Devices (Code: KIR)

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.

K973212FRESH CELLS WI-38Diagnostic Hybrids, Inc.K973210FRESH CELLS NCI H292Diagnostic Hybrids, Inc.K973209FRESH CELLS VERODiagnostic Hybrids, Inc.K973211FRESH CELLS MV1LUDiagnostic Hybrids, Inc.K973213FRESH CELLS LLC-MK2Diagnostic Hybrids, Inc.K973214FRESH CELLS HFFDiagnostic Hybrids, Inc.

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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