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FDA 510(k)

NUCLITRYP(TM)(I125)-HUMAN PANCREA CATH TRY RAD KIT

K-Number: K932406 · 1993-12-02

ApplicantNuclear Diagnostics, Inc.
Decision Date1993-12-02
Product CodeJNO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

NUCLITRYP(TM)(I125)-HUMAN PANCREA CATH TRY RAD KIT is the device name listed in this FDA 510(k) record. The listed applicant is Nuclear Diagnostics, Inc.. It received FDA 510(k) clearance on 1993-12-02 under 510(k) number K932406. The device is classified under product code JNO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUCLITRYP(TM)(I125)-HUMAN PANCREA CATH TRY RAD KIT?

NUCLITRYP(TM)(I125)-HUMAN PANCREA CATH TRY RAD KIT is a medical device that received FDA 510(k) clearance on 1993-12-02. The listed applicant is Nuclear Diagnostics, Inc.. The 510(k) number is K932406.

When did NUCLITRYP(TM)(I125)-HUMAN PANCREA CATH TRY RAD KIT receive FDA 510(k) clearance?

NUCLITRYP(TM)(I125)-HUMAN PANCREA CATH TRY RAD KIT received FDA 510(k) clearance on 1993-12-02, under 510(k) number K932406.

Who is the listed applicant for NUCLITRYP(TM)(I125)-HUMAN PANCREA CATH TRY RAD KIT?

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

What is the FDA product code for NUCLITRYP(TM)(I125)-HUMAN PANCREA CATH TRY RAD KIT?

The FDA product code for NUCLITRYP(TM)(I125)-HUMAN PANCREA CATH TRY RAD KIT is JNO.

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Other records listing Nuclear Diagnostics, 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.

K923917ELIPASE HUMAN PANCREATIC LIPASE ENZYMEIMMUNOASSAYK872177TIPSEP-CORTISOL RIA DIAGNOSTIC KITK862312ENZLIPASE, ENZYMATIC LIPASE KITK860472NUCLEAR LASER ALIGNMENT SYSTEM FOR CARDIC STRESSK861735TIPSEP-TBG ASSAYK852291TIPSEP DIGOXIN RIA

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Related Devices (Code: JNO)

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.

K110274AUTODELFIA NEONATAL IRT KITWallac Oy, A Subsidiary of Perkinelmer, Inc.K102419GSP NEONATAL IRT KIT (3306-001U)Wallac Oy, Subsidiary of PerkinelmerK883011MRI NEO-TRYP TRYPSIN RIAMicrobiological Research Corp.K861097TRYPSIN RIA KITMicroanalytic Research, Inc.K811805TRYPIN (125I) RIA KITBd Becton Dickinson Vacutainer Systems PreanalyticK791202RIA KIT FOR TRYPSINCis Radiopharmaceuticals, 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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