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FDA 510(k)

FRESH CELLS MULTI-WELL & SHELL VIAL CULTURES

K-Number: K962306 · 1996-08-29

ApplicantDiagnostic Hybrids, Inc.
Decision Date1996-08-29
Product CodeKIR
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

FRESH CELLS MULTI-WELL & SHELL VIAL CULTURES is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Hybrids, Inc.. It received FDA 510(k) clearance on 1996-08-29 under 510(k) number K962306. 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 FRESH CELLS MULTI-WELL & SHELL VIAL CULTURES?

FRESH CELLS MULTI-WELL & SHELL VIAL CULTURES is a medical device that received FDA 510(k) clearance on 1996-08-29. The listed applicant is Diagnostic Hybrids, Inc.. The 510(k) number is K962306.

When did FRESH CELLS MULTI-WELL & SHELL VIAL CULTURES receive FDA 510(k) clearance?

FRESH CELLS MULTI-WELL & SHELL VIAL CULTURES received FDA 510(k) clearance on 1996-08-29, under 510(k) number K962306.

Who is the listed applicant for FRESH CELLS MULTI-WELL & SHELL VIAL CULTURES?

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

What is the FDA product code for FRESH CELLS MULTI-WELL & SHELL VIAL CULTURES?

The FDA product code for FRESH CELLS MULTI-WELL & SHELL VIAL CULTURES is KIR.

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Other records listing Diagnostic Hybrids, Inc. as applicant

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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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