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FDA 510(k)

PROBE REFILL KIT

K-Number: K911073 · 1991-06-06

ApplicantInterspec, Inc.
Decision Date1991-06-06
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PROBE REFILL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Interspec, Inc.. It received FDA 510(k) clearance on 1991-06-06 under 510(k) number K911073. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROBE REFILL KIT?

PROBE REFILL KIT is a medical device that received FDA 510(k) clearance on 1991-06-06. The listed applicant is Interspec, Inc.. The 510(k) number is K911073.

When did PROBE REFILL KIT receive FDA 510(k) clearance?

PROBE REFILL KIT received FDA 510(k) clearance on 1991-06-06, under 510(k) number K911073.

Who is the listed applicant for PROBE REFILL KIT?

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

What is the FDA product code for PROBE REFILL KIT?

The FDA product code for PROBE REFILL KIT is ITX.

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Related Devices (Code: ITX)

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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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