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FDA 510(k)

NICOLET DISPOSABLE PRASS PROBE

K-Number: K873964 · 1987-11-20

ApplicantNicolet Biomedical Instruments
Decision Date1987-11-20
Product CodeETN
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

NICOLET DISPOSABLE PRASS PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Nicolet Biomedical Instruments. It received FDA 510(k) clearance on 1987-11-20 under 510(k) number K873964. The device is classified under product code ETN. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NICOLET DISPOSABLE PRASS PROBE?

NICOLET DISPOSABLE PRASS PROBE is a medical device that received FDA 510(k) clearance on 1987-11-20. The listed applicant is Nicolet Biomedical Instruments. The 510(k) number is K873964.

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

NICOLET DISPOSABLE PRASS PROBE received FDA 510(k) clearance on 1987-11-20, under 510(k) number K873964.

Who is the listed applicant for NICOLET DISPOSABLE PRASS PROBE?

The FDA 510(k) record lists Nicolet Biomedical Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NICOLET DISPOSABLE PRASS PROBE?

The FDA product code for NICOLET DISPOSABLE PRASS PROBE is ETN.

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Other records listing Nicolet Biomedical Instruments as applicant

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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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