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FDA 510(k)

POOLE TIP SUCTION PROBE

K-Number: K915762 · 1992-03-13

ApplicantO.R. Concepts, Inc.
Decision Date1992-03-13
Product CodeGCI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

POOLE TIP SUCTION PROBE is the device name listed in this FDA 510(k) record. The listed applicant is O.R. Concepts, Inc.. It received FDA 510(k) clearance on 1992-03-13 under 510(k) number K915762. The device is classified under product code GCI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POOLE TIP SUCTION PROBE?

POOLE TIP SUCTION PROBE is a medical device that received FDA 510(k) clearance on 1992-03-13. The listed applicant is O.R. Concepts, Inc.. The 510(k) number is K915762.

When did POOLE TIP SUCTION PROBE receive FDA 510(k) clearance?

POOLE TIP SUCTION PROBE received FDA 510(k) clearance on 1992-03-13, under 510(k) number K915762.

Who is the listed applicant for POOLE TIP SUCTION PROBE?

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

What is the FDA product code for POOLE TIP SUCTION PROBE?

The FDA product code for POOLE TIP SUCTION PROBE is GCI.

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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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