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FDA 510(k)

NASSAL PRESSURE/FLOW RECORDER

K-Number: K772193 · 1977-12-02

ApplicantAdco Labs.
Decision Date1977-12-02
Product CodeETL
DecisionSubstantially Equivalent

Device Summary

NASSAL PRESSURE/FLOW RECORDER is the device name listed in this FDA 510(k) record. The listed applicant is Adco Labs.. It received FDA 510(k) clearance on 1977-12-02 under 510(k) number K772193. The device is classified under product code ETL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NASSAL PRESSURE/FLOW RECORDER?

NASSAL PRESSURE/FLOW RECORDER is a medical device that received FDA 510(k) clearance on 1977-12-02. The listed applicant is Adco Labs.. The 510(k) number is K772193.

When did NASSAL PRESSURE/FLOW RECORDER receive FDA 510(k) clearance?

NASSAL PRESSURE/FLOW RECORDER received FDA 510(k) clearance on 1977-12-02, under 510(k) number K772193.

Who is the listed applicant for NASSAL PRESSURE/FLOW RECORDER?

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

What is the FDA product code for NASSAL PRESSURE/FLOW RECORDER?

The FDA product code for NASSAL PRESSURE/FLOW RECORDER is ETL.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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