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FDA 510(k)

16 X 125 MM TEST TUBE, CATALOG #01-111

K-Number: K930392 · 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 #01-111 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 K930392. 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 #01-111?

16 X 125 MM TEST TUBE, CATALOG #01-111 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 K930392.

When did 16 X 125 MM TEST TUBE, CATALOG #01-111 receive FDA 510(k) clearance?

16 X 125 MM TEST TUBE, CATALOG #01-111 received FDA 510(k) clearance on 1993-03-24, under 510(k) number K930392.

Who is the listed applicant for 16 X 125 MM TEST TUBE, CATALOG #01-111?

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 #01-111?

The FDA product code for 16 X 125 MM TEST TUBE, CATALOG #01-111 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 MEDIUMK93039716 X 125 MM TEST TUBE, CATALOGK930395ONE DRAM SHELL VIAL, CATALOG #02-461K93039025 CM2, 75 CM2, 125 CM2 FLASK, CATALOG #03-291K930393ONE 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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