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FDA 510(k)

NCI-H292 CELL CULTURE

K-Number: K951461 · 1996-05-22

ApplicantViromed Laboratories, Inc.
Decision Date1996-05-22
Product CodeKIR
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

NCI-H292 CELL CULTURE is the device name listed in this FDA 510(k) record. The listed applicant is Viromed Laboratories, Inc.. It received FDA 510(k) clearance on 1996-05-22 under 510(k) number K951461. 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 NCI-H292 CELL CULTURE?

NCI-H292 CELL CULTURE is a medical device that received FDA 510(k) clearance on 1996-05-22. The listed applicant is Viromed Laboratories, Inc.. The 510(k) number is K951461.

When did NCI-H292 CELL CULTURE receive FDA 510(k) clearance?

NCI-H292 CELL CULTURE received FDA 510(k) clearance on 1996-05-22, under 510(k) number K951461.

Who is the listed applicant for NCI-H292 CELL CULTURE?

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

What is the FDA product code for NCI-H292 CELL CULTURE?

The FDA product code for NCI-H292 CELL CULTURE is KIR.

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Other records listing Viromed Laboratories, 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.

K951440LLC-MK2 (MONKEY KIDNEY, MACACA MULATA) CELL CULTUREK871613BUFFALO GREEN MONKEY KIDNEY CELLSK862555HUMAN EPITHELOID CERVIX CARCINOMA CELLS (HELA)K861373HUMAN LUNG CARCINOMA CELLS (A549)K853695RESPIRATORY SYNCYTIAL VIRUS ID REAGENTK852395MINK LUNG

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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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