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FDA 510(k)

NORMAL ANGIOTENSIN CONVERTING ENZYME CONTROL

K-Number: K925906 · 1993-02-18

ApplicantAnalytical Control Systems, Inc.
Decision Date1993-02-18
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

NORMAL ANGIOTENSIN CONVERTING ENZYME CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Analytical Control Systems, Inc.. It received FDA 510(k) clearance on 1993-02-18 under 510(k) number K925906. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORMAL ANGIOTENSIN CONVERTING ENZYME CONTROL?

NORMAL ANGIOTENSIN CONVERTING ENZYME CONTROL is a medical device that received FDA 510(k) clearance on 1993-02-18. The listed applicant is Analytical Control Systems, Inc.. The 510(k) number is K925906.

When did NORMAL ANGIOTENSIN CONVERTING ENZYME CONTROL receive FDA 510(k) clearance?

NORMAL ANGIOTENSIN CONVERTING ENZYME CONTROL received FDA 510(k) clearance on 1993-02-18, under 510(k) number K925906.

Who is the listed applicant for NORMAL ANGIOTENSIN CONVERTING ENZYME CONTROL?

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

What is the FDA product code for NORMAL ANGIOTENSIN CONVERTING ENZYME CONTROL?

The FDA product code for NORMAL ANGIOTENSIN CONVERTING ENZYME CONTROL is JJX.

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Other records listing Analytical Control Systems, Inc. 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.

K961892SPECKTIN-LA TEST SETK941115ACS CARDIO-TROL CONTROLK940272ACS NORMAL ANGIOTENSIN CONVERTING ENZYME CONTROLK940397ACS O DILVENT PROTEIN DILUTION MATRIXK930477ACS ANGIOTENSIN CONVERTING ENZYME (ACE) CALIBRATORK926012ACS APCT REAGENT, MODIFIED

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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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