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FDA 510(k)

MIC-CONCEPT VIEWBOX

K-Number: K853745 · 1985-09-19

ApplicantMicrotech Medical Systems, Inc.
Decision Date1985-09-19
Product CodeLIB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MIC-CONCEPT VIEWBOX is the device name listed in this FDA 510(k) record. The listed applicant is Microtech Medical Systems, Inc.. It received FDA 510(k) clearance on 1985-09-19 under 510(k) number K853745. The device is classified under product code LIB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIC-CONCEPT VIEWBOX?

MIC-CONCEPT VIEWBOX is a medical device that received FDA 510(k) clearance on 1985-09-19. The listed applicant is Microtech Medical Systems, Inc.. The 510(k) number is K853745.

When did MIC-CONCEPT VIEWBOX receive FDA 510(k) clearance?

MIC-CONCEPT VIEWBOX received FDA 510(k) clearance on 1985-09-19, under 510(k) number K853745.

Who is the listed applicant for MIC-CONCEPT VIEWBOX?

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

What is the FDA product code for MIC-CONCEPT VIEWBOX?

The FDA product code for MIC-CONCEPT VIEWBOX is LIB.

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Other records listing Microtech Medical Systems, 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.

K935485FAS FASTIDIOUS MIC PANELK901598FASTIDIOUS MIC PANELK896332SUPPLEMENT TO ANAEROBIC MIC PANELK884831ANAEROBIC MIC PANELK863847MIC - CONCEPT(TM) RX-2K861774QUADRA-TITER (TM) I.D. (MODIFICATION)

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Related Devices (Code: LIB)

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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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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