Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SINGLE VIAL AMYLASE PNP TEST

K-Number: K823462 · 1982-12-28

Decision Date1982-12-28
Product CodeJFJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SINGLE VIAL AMYLASE PNP TEST is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Mannheim Corp.. It received FDA 510(k) clearance on 1982-12-28 under 510(k) number K823462. The device is classified under product code JFJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SINGLE VIAL AMYLASE PNP TEST?

SINGLE VIAL AMYLASE PNP TEST is a medical device that received FDA 510(k) clearance on 1982-12-28. The listed applicant is Boehringer Mannheim Corp.. The 510(k) number is K823462.

When did SINGLE VIAL AMYLASE PNP TEST receive FDA 510(k) clearance?

SINGLE VIAL AMYLASE PNP TEST received FDA 510(k) clearance on 1982-12-28, under 510(k) number K823462.

Who is the listed applicant for SINGLE VIAL AMYLASE PNP TEST?

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

What is the FDA product code for SINGLE VIAL AMYLASE PNP TEST?

The FDA product code for SINGLE VIAL AMYLASE PNP TEST is JFJ.

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.

Other records listing Boehringer Mannheim 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.

View all 340 devices →

Related Devices (Code: JFJ)

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.

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.

↑