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FDA 510(k)

A549 CELL CULTURE

K-Number: K955921 · 1996-02-16

ApplicantViratest Intl., Inc.
Decision Date1996-02-16
Product CodeKIR
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

A549 CELL CULTURE is the device name listed in this FDA 510(k) record. The listed applicant is Viratest Intl., Inc.. It received FDA 510(k) clearance on 1996-02-16 under 510(k) number K955921. 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 A549 CELL CULTURE?

A549 CELL CULTURE is a medical device that received FDA 510(k) clearance on 1996-02-16. The listed applicant is Viratest Intl., Inc.. The 510(k) number is K955921.

When did A549 CELL CULTURE receive FDA 510(k) clearance?

A549 CELL CULTURE received FDA 510(k) clearance on 1996-02-16, under 510(k) number K955921.

Who is the listed applicant for A549 CELL CULTURE?

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

What is the FDA product code for A549 CELL CULTURE?

The FDA product code for A549 CELL CULTURE is KIR.

Related Clinical Trials

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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Other records listing Viratest 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.

K952727MRC-5 CELL CULTURE VIALK931922DIADOT(TM) VIRUS/CHLAMYDIA TRANSPORT

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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