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FDA 510(k)

PALPATION PROBE

K-Number: K911159 · 1991-03-29

ApplicantNorthgate Technologies, Inc.
Decision Date1991-03-29
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PALPATION PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Northgate Technologies, Inc.. It received FDA 510(k) clearance on 1991-03-29 under 510(k) number K911159. The device is classified under product code GEN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PALPATION PROBE?

PALPATION PROBE is a medical device that received FDA 510(k) clearance on 1991-03-29. The listed applicant is Northgate Technologies, Inc.. The 510(k) number is K911159.

When did PALPATION PROBE receive FDA 510(k) clearance?

PALPATION PROBE received FDA 510(k) clearance on 1991-03-29, under 510(k) number K911159.

Who is the listed applicant for PALPATION PROBE?

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

What is the FDA product code for PALPATION PROBE?

The FDA product code for PALPATION PROBE is GEN.

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Other records listing Northgate Technologies, Inc. as applicant

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Related Devices (Code: GEN)

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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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