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FDA 510(k)

TRAY, PRESSURE, INTRACOMPARTMENTAL,WICK

K-Number: K770776 · 1977-08-04

ApplicantCutter Laboratories, Inc.
Decision Date1977-08-04
Product Code
DecisionSubstantially Equivalent

Device Summary

TRAY, PRESSURE, INTRACOMPARTMENTAL,WICK is the device name listed in this FDA 510(k) record. The listed applicant is Cutter Laboratories, Inc.. It received FDA 510(k) clearance on 1977-08-04 under 510(k) number K770776. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRAY, PRESSURE, INTRACOMPARTMENTAL,WICK?

TRAY, PRESSURE, INTRACOMPARTMENTAL,WICK is a medical device that received FDA 510(k) clearance on 1977-08-04. The listed applicant is Cutter Laboratories, Inc.. The 510(k) number is K770776.

When did TRAY, PRESSURE, INTRACOMPARTMENTAL,WICK receive FDA 510(k) clearance?

TRAY, PRESSURE, INTRACOMPARTMENTAL,WICK received FDA 510(k) clearance on 1977-08-04, under 510(k) number K770776.

Who is the listed applicant for TRAY, PRESSURE, INTRACOMPARTMENTAL,WICK?

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

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Other records listing Cutter Laboratories, Inc. as applicant

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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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