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FDA 510(k)

MICROTEK PROBE DRAPE

K-Number: K882724 · 1988-08-03

ApplicantMicrobio-Medics, Inc.
Decision Date1988-08-03
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICROTEK PROBE DRAPE is the device name listed in this FDA 510(k) record. The listed applicant is Microbio-Medics, Inc.. It received FDA 510(k) clearance on 1988-08-03 under 510(k) number K882724. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROTEK PROBE DRAPE?

MICROTEK PROBE DRAPE is a medical device that received FDA 510(k) clearance on 1988-08-03. The listed applicant is Microbio-Medics, Inc.. The 510(k) number is K882724.

When did MICROTEK PROBE DRAPE receive FDA 510(k) clearance?

MICROTEK PROBE DRAPE received FDA 510(k) clearance on 1988-08-03, under 510(k) number K882724.

Who is the listed applicant for MICROTEK PROBE DRAPE?

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

What is the FDA product code for MICROTEK PROBE DRAPE?

The FDA product code for MICROTEK PROBE DRAPE is KKX.

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Other records listing Microbio-Medics, Inc. as applicant

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Related Devices (Code: KKX)

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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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