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FDA 510(k)

PHOSPHORUS IL

K-Number: K820832 · 1982-04-15

ApplicantAmerican Monitor Corp.
Decision Date1982-04-15
Product CodeCED
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PHOSPHORUS IL is the device name listed in this FDA 510(k) record. The listed applicant is American Monitor Corp.. It received FDA 510(k) clearance on 1982-04-15 under 510(k) number K820832. The device is classified under product code CED. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHOSPHORUS IL?

PHOSPHORUS IL is a medical device that received FDA 510(k) clearance on 1982-04-15. The listed applicant is American Monitor Corp.. The 510(k) number is K820832.

When did PHOSPHORUS IL receive FDA 510(k) clearance?

PHOSPHORUS IL received FDA 510(k) clearance on 1982-04-15, under 510(k) number K820832.

Who is the listed applicant for PHOSPHORUS IL?

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

What is the FDA product code for PHOSPHORUS IL?

The FDA product code for PHOSPHORUS IL is CED.

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Other records listing American Monitor Corp. 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.

K896000ASPARTATE AMINOTRANFERASE (AST)K895999PHOSPHORUSK896001ALANINE AMINOTRANSFERASE (ALT)K895423ACCESS CHEMISTRY ANALYZERK893137EXCEL (TM) CHEMISTRY ANALYZERK892331ENZYMATIC UREA NITROGEN REAGENT SET

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Related Devices (Code: CED)

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.

K894288PHOSPHORUS TEST ITEM NUMBER 65416Em Diagnostic Systems, Inc.K840151EKTACHEM CLINICAL CHEM. SLIDESEastman Kodak CompanyK833710BTC URINE LH ASSAYBtc Diagnostics, Inc.K812670SANDARE FAST 340 PHOSPHORUS PROCEDURESandare Chemical Co., Inc.K811864SIGMA PROCEDURE 265-UVSigma Chemical Co.K811222INORGANIC PHOSPHORUS REAGENTSConnecticut Diagnostics, Ltd.

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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