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FDA 510(k)

MICROSEPT 60/20

K-Number: K890844 · 1989-06-07

ApplicantArbor Technologies, Inc.
Decision Date1989-06-07
Product CodeCAK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MICROSEPT 60/20 is the device name listed in this FDA 510(k) record. The listed applicant is Arbor Technologies, Inc.. It received FDA 510(k) clearance on 1989-06-07 under 510(k) number K890844. The device is classified under product code CAK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROSEPT 60/20?

MICROSEPT 60/20 is a medical device that received FDA 510(k) clearance on 1989-06-07. The listed applicant is Arbor Technologies, Inc.. The 510(k) number is K890844.

When did MICROSEPT 60/20 receive FDA 510(k) clearance?

MICROSEPT 60/20 received FDA 510(k) clearance on 1989-06-07, under 510(k) number K890844.

Who is the listed applicant for MICROSEPT 60/20?

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

What is the FDA product code for MICROSEPT 60/20?

The FDA product code for MICROSEPT 60/20 is CAK.

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Other records listing Arbor Technologies, 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: CAK)

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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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