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FDA 510(k)

ANAEROBE RAPID CHROMOGENIC ID PANEL

K-Number: K862332 · 1986-08-27

ApplicantAmerican Micro Scan
Decision Date1986-08-27
Product CodeJSP
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ANAEROBE RAPID CHROMOGENIC ID PANEL is the device name listed in this FDA 510(k) record. The listed applicant is American Micro Scan. It received FDA 510(k) clearance on 1986-08-27 under 510(k) number K862332. The device is classified under product code JSP. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANAEROBE RAPID CHROMOGENIC ID PANEL?

ANAEROBE RAPID CHROMOGENIC ID PANEL is a medical device that received FDA 510(k) clearance on 1986-08-27. The listed applicant is American Micro Scan. The 510(k) number is K862332.

When did ANAEROBE RAPID CHROMOGENIC ID PANEL receive FDA 510(k) clearance?

ANAEROBE RAPID CHROMOGENIC ID PANEL received FDA 510(k) clearance on 1986-08-27, under 510(k) number K862332.

Who is the listed applicant for ANAEROBE RAPID CHROMOGENIC ID PANEL?

The FDA 510(k) record lists American Micro Scan as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANAEROBE RAPID CHROMOGENIC ID PANEL?

The FDA product code for ANAEROBE RAPID CHROMOGENIC ID PANEL is JSP.

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Other records listing American Micro Scan 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.

K864662CHLAMYDIAE FLUOR. AB TEST FOR DETECTION IN SMEARSK870029IMMUNOSCAN(TM) DIRECT STREPTOCOCCUS PNEUMONIAEK863776MICRODILUTION MIC PANELSK864674MICRODILUTION IDENTIFICATION PANELSK864389CHLAMYDIAE FLOURESCENT MONOCLONAL ANTIBODY TESTK863038GRAM POSITIVE FLUORESCENT IDENTIFICATION PANEL

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Related Devices (Code: JSP)

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.

K945487LYFO(TM) DIFFERENTIAL DISKMicrobiologics, Inc.K945489LYFO(TM) DIFFERENTIAL DISKMicrobiologics, Inc.K945488LYFO(TM) DIFFERENTIAL DISKMicrobiologics, Inc.K944528BBLCRYSTAL ANAEROBE ID SYSTEMBecton Dickinson Microbiology SystemsK910666VITEK ANAEROBE IDENTIFICATION CARD, MODIFICATIONVitek Systems, Inc.K900996VITEK ANAEROBE IDENTIFICATION CARDVitek Systems, 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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