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FDA 510(k)

CONTAINER SYSTEM

K-Number: K831068 · 1983-05-09

ApplicantAdler Instrument Co.
Decision Date1983-05-09
Product Code
DecisionSubstantially Equivalent

Device Summary

CONTAINER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Adler Instrument Co.. It received FDA 510(k) clearance on 1983-05-09 under 510(k) number K831068. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTAINER SYSTEM?

CONTAINER SYSTEM is a medical device that received FDA 510(k) clearance on 1983-05-09. The listed applicant is Adler Instrument Co.. The 510(k) number is K831068.

When did CONTAINER SYSTEM receive FDA 510(k) clearance?

CONTAINER SYSTEM received FDA 510(k) clearance on 1983-05-09, under 510(k) number K831068.

Who is the listed applicant for CONTAINER SYSTEM?

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

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Adler Instrument Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K910170MAXI-FLOW SUCTION SET 12 FT.K910171MAXI-FLOW SUCTION SET W/Y CONNECTORK903209MAXI-FLOW INSUFFLATOR TUBING SET W/FILTERK903208MAXI-FLOW INSUFFLATOR TUBING SETK900913ADLER DISPOSABLE BIPOLAR CORDK841723ADLER CUSTOM PROCEDURE PACKS

View all 8 devices →

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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