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FDA 510(k)

MILENIA PAP IRMA CATALOG #: MKPA1, X

K-Number: K902937 · 1990-09-21

ApplicantDiagnostic Products Corp.
Decision Date1990-09-21
Product CodeJFH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MILENIA PAP IRMA CATALOG #: MKPA1, X is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Products Corp.. It received FDA 510(k) clearance on 1990-09-21 under 510(k) number K902937. The device is classified under product code JFH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MILENIA PAP IRMA CATALOG #: MKPA1, X?

MILENIA PAP IRMA CATALOG #: MKPA1, X is a medical device that received FDA 510(k) clearance on 1990-09-21. The listed applicant is Diagnostic Products Corp.. The 510(k) number is K902937.

When did MILENIA PAP IRMA CATALOG #: MKPA1, X receive FDA 510(k) clearance?

MILENIA PAP IRMA CATALOG #: MKPA1, X received FDA 510(k) clearance on 1990-09-21, under 510(k) number K902937.

Who is the listed applicant for MILENIA PAP IRMA CATALOG #: MKPA1, X?

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

What is the FDA product code for MILENIA PAP IRMA CATALOG #: MKPA1, X?

The FDA product code for MILENIA PAP IRMA CATALOG #: MKPA1, X is JFH.

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 Diagnostic Products 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.

K063045IMMULITE 2000, IMMULITE 2500 VANCOMYCINK034055IMMULITE 2500 CK-MB, 2500 MYOGLOBIN, 2500 STAT TROPONIN IK033234IMMULITE 2500 AUTOMATED IMMUNOASSAY ANALYZERK032881IMMULITE/IMMULITE 1000 TOTAL TESTOSTERONE AND IMMULITE 2000 TOTAL TESTOSTERONEK023152IMMULITE 2000 ALLERGEN-SPECIFIC IGEK023304IMMULITE/IMMULITE 1000 CALCITONIN, MODEL LKCL AND IMMULITE 2000 CALCITONIN, MODEL L2KCL

View all 321 devices →

Related Devices (Code: JFH)

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.

K000257IMMULITE 2000 PAP, MODELS L2KPA2, L2KPA6Diagnostic Products Corp.K981573UBI MAGIWEL PAP (PROSTATIC ACID PHOSPHATASE) EIA QUANTITATVEUnited Biotech, Inc.K964756PROSTATIC ACID PHOSPHATASE REAGENT TEST/PROSTATIC ACID PHOSPHATASE REAGENT KITWano-Tech Corp.K931701IMMULITE PAPDiagnostic Products Corp.K925377IMX PAPAbbott LaboratoriesK921745HYBRITECH STRATUS PAP FLUOROMETRIC ENZYME IMMUNOHybritech, Inc.

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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