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FDA 510(k)

FITC MURINE MONOCLONAL ANTI-HERPES TYPE 1 IGG

K-Number: K881180 · 1988-05-13

ApplicantWhittaker Bioproducts, Inc.
Decision Date1988-05-13
Product CodeGQN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

FITC MURINE MONOCLONAL ANTI-HERPES TYPE 1 IGG is the device name listed in this FDA 510(k) record. The listed applicant is Whittaker Bioproducts, Inc.. It received FDA 510(k) clearance on 1988-05-13 under 510(k) number K881180. The device is classified under product code GQN. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FITC MURINE MONOCLONAL ANTI-HERPES TYPE 1 IGG?

FITC MURINE MONOCLONAL ANTI-HERPES TYPE 1 IGG is a medical device that received FDA 510(k) clearance on 1988-05-13. The listed applicant is Whittaker Bioproducts, Inc.. The 510(k) number is K881180.

When did FITC MURINE MONOCLONAL ANTI-HERPES TYPE 1 IGG receive FDA 510(k) clearance?

FITC MURINE MONOCLONAL ANTI-HERPES TYPE 1 IGG received FDA 510(k) clearance on 1988-05-13, under 510(k) number K881180.

Who is the listed applicant for FITC MURINE MONOCLONAL ANTI-HERPES TYPE 1 IGG?

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

What is the FDA product code for FITC MURINE MONOCLONAL ANTI-HERPES TYPE 1 IGG?

The FDA product code for FITC MURINE MONOCLONAL ANTI-HERPES TYPE 1 IGG is GQN.

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Other records listing Whittaker Bioproducts, 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.

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Related Devices (Code: GQN)

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.

K070265DIAGNOSTIC HYBRIDS' D3 DFA HERPES SIMPLEX VIRUS IDENTIFICATION AND TYPING KIT, MODEL 01-090000Diagnostic Hybrids, Inc.K063798DIAGNOSTIC HYBRIDS' D3 DFA HERPES SIMPLEX VIRUS IDENTIFICATION KIT, MODEL 01-080000Diagnostic Hybrids, Inc.K991880LIGHT DIAGNOSTICS SIMULFLUOR HSV 1/2 IMMUNOFLUORECENCE ASSAYLight DiagnosticsK971662ELVIS HSV ID/TYPING TEST SYSTEMDiagnostic Hybrids, Inc.K971101HSV-2 ANTIGEN CONTROL SLIDESViral Antigens, Inc.K964874HSV-1 ANTIGEN CONTROL SLIDESViral Antigens, 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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