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FDA 510(k)

ADLER CUSTOM PROCEDURE PACKS

K-Number: K841723 · 1984-08-01

ApplicantAdler Instrument Co.
Decision Date1984-08-01
Product Code
DecisionSubstantially Equivalent

Device Summary

ADLER CUSTOM PROCEDURE PACKS 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 1984-08-01 under 510(k) number K841723. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADLER CUSTOM PROCEDURE PACKS?

ADLER CUSTOM PROCEDURE PACKS is a medical device that received FDA 510(k) clearance on 1984-08-01. The listed applicant is Adler Instrument Co.. The 510(k) number is K841723.

When did ADLER CUSTOM PROCEDURE PACKS receive FDA 510(k) clearance?

ADLER CUSTOM PROCEDURE PACKS received FDA 510(k) clearance on 1984-08-01, under 510(k) number K841723.

Who is the listed applicant for ADLER CUSTOM PROCEDURE PACKS?

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 CORDK833264ADLER STEAM INDICATOR-GAS INDICATOR

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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