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)

TRANS 2000

K-Number: K771018 · 1977-07-14

Decision Date1977-07-14
Product CodeINK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TRANS 2000 is the device name listed in this FDA 510(k) record. The listed applicant is Hamilton Industries, Inc.. It received FDA 510(k) clearance on 1977-07-14 under 510(k) number K771018. The device is classified under product code INK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANS 2000?

TRANS 2000 is a medical device that received FDA 510(k) clearance on 1977-07-14. The listed applicant is Hamilton Industries, Inc.. The 510(k) number is K771018.

When did TRANS 2000 receive FDA 510(k) clearance?

TRANS 2000 received FDA 510(k) clearance on 1977-07-14, under 510(k) number K771018.

Who is the listed applicant for TRANS 2000?

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

What is the FDA product code for TRANS 2000?

The FDA product code for TRANS 2000 is INK.

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 Hamilton Industries, 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.

Related Devices (Code: INK)

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.

↑