FDA 510(k)

RIA KIT FOR TRYPSIN

K-Number: K791202 · 1979-11-05

Decision Date1979-11-05

Product CodeJNO

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

RIA KIT FOR TRYPSIN is the device name listed in this FDA 510(k) record. The listed applicant is Cis Radiopharmaceuticals, Inc.. It received FDA 510(k) clearance on 1979-11-05 under 510(k) number K791202. 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 RIA KIT FOR TRYPSIN?

RIA KIT FOR TRYPSIN is a medical device that received FDA 510(k) clearance on 1979-11-05. The listed applicant is Cis Radiopharmaceuticals, Inc.. The 510(k) number is K791202.

When did RIA KIT FOR TRYPSIN receive FDA 510(k) clearance?

RIA KIT FOR TRYPSIN received FDA 510(k) clearance on 1979-11-05, under 510(k) number K791202.

Who is the listed applicant for RIA KIT FOR TRYPSIN?

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

What is the FDA product code for RIA KIT FOR TRYPSIN?

The FDA product code for RIA KIT FOR TRYPSIN is JNO.

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Other records listing Cis Radiopharmaceuticals, Inc. as applicant

K791860FERRITIN RIA KIT K792063FOLLICLE STIMULATING HORMONE (FSH) KIT K792000LUTEINIZING HORMONE (LH) RIA K791051PROGESTERONE RADIOIMMUNOASSAY KIT K790003RIA KIT, PROLACTIN K780982KITS, RIA, MYOGLOBIN, HUMAN, MEASUREMENT

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Related Devices (Code: JNO)

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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.