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)

CHEMTAB

K-Number: K790772 · 1979-06-15

Decision Date1979-06-15
Product CodeJIM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CHEMTAB 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 1979-06-15 under 510(k) number K790772. The device is classified under product code JIM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHEMTAB?

CHEMTAB is a medical device that received FDA 510(k) clearance on 1979-06-15. The listed applicant is Boehringer Mannheim Corp.. The 510(k) number is K790772.

When did CHEMTAB receive FDA 510(k) clearance?

CHEMTAB received FDA 510(k) clearance on 1979-06-15, under 510(k) number K790772.

Who is the listed applicant for CHEMTAB?

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 CHEMTAB?

The FDA product code for CHEMTAB is JIM.

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: JIM)

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.

↑