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FDA 510(k)

RIA TEST, NORDICALB HPL

K-Number: K782099 · 1979-01-10

ApplicantNordiclab Intl.
Decision Date1979-01-10
Product CodeJMF
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RIA TEST, NORDICALB HPL is the device name listed in this FDA 510(k) record. The listed applicant is Nordiclab Intl.. It received FDA 510(k) clearance on 1979-01-10 under 510(k) number K782099. The device is classified under product code JMF. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIA TEST, NORDICALB HPL?

RIA TEST, NORDICALB HPL is a medical device that received FDA 510(k) clearance on 1979-01-10. The listed applicant is Nordiclab Intl.. The 510(k) number is K782099.

When did RIA TEST, NORDICALB HPL receive FDA 510(k) clearance?

RIA TEST, NORDICALB HPL received FDA 510(k) clearance on 1979-01-10, under 510(k) number K782099.

Who is the listed applicant for RIA TEST, NORDICALB HPL?

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

What is the FDA product code for RIA TEST, NORDICALB HPL?

The FDA product code for RIA TEST, NORDICALB HPL is JMF.

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Other records listing Nordiclab Intl. 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.

K801988NORDICLAB PROSTATIC ACID PHOSPHATASE RIAK801989NORDICLAB FERRITIN IRMA TESTK800920NORDICLAB ESTRADIOL RIA TESTK800922NORDICLAB PROGESTERONE RIA TESTK800921NORDICLAB TESTOSTERONE RIA TESTK792189NORDICLAB TOTAL ESTRIOL RIA TEST

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Related Devices (Code: JMF)

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.

K944933IMMULITE (HPL) (HUMAN PLACENTAL PLACTOGEN)Diagnostic Products Corp.K840588AMERLEX HUMAN PLACENTAL LACTOGENAmersham Corp.K823292IMMOPHASE TM HPL RADIOIMMUNOASSAYCorning Medical & ScientificK823201HUMAN PLACENTAL LACTOGEN KITDiagnostic Products Corp.K811370NATAL-TEC HPLArmkel, LLCK802454GESTE FOLLOW KIT DETERM. OF HPLSyn-Kit, 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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