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FDA 510(k)

DISPOSABLE SUCTION PROBE

K-Number: K942061 · 1994-05-16

ApplicantUnited States Surgical, A Division of Tyco Healthc
Decision Date1994-05-16
Product CodeJOL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE SUCTION PROBE is the device name listed in this FDA 510(k) record. The listed applicant is United States Surgical, A Division of Tyco Healthc. It received FDA 510(k) clearance on 1994-05-16 under 510(k) number K942061. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE SUCTION PROBE?

DISPOSABLE SUCTION PROBE is a medical device that received FDA 510(k) clearance on 1994-05-16. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K942061.

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

DISPOSABLE SUCTION PROBE received FDA 510(k) clearance on 1994-05-16, under 510(k) number K942061.

Who is the listed applicant for DISPOSABLE SUCTION PROBE?

The FDA 510(k) record lists United States Surgical, A Division of Tyco Healthc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE SUCTION PROBE?

The FDA product code for DISPOSABLE SUCTION PROBE is JOL.

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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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