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)

THAYER MIP ADAPTER

K-Number: K904917 · 1991-01-28

Decision Date1991-01-28
Product CodeBXR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

THAYER MIP ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Thayer Medical Corp.. It received FDA 510(k) clearance on 1991-01-28 under 510(k) number K904917. The device is classified under product code BXR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THAYER MIP ADAPTER?

THAYER MIP ADAPTER is a medical device that received FDA 510(k) clearance on 1991-01-28. The listed applicant is Thayer Medical Corp.. The 510(k) number is K904917.

When did THAYER MIP ADAPTER receive FDA 510(k) clearance?

THAYER MIP ADAPTER received FDA 510(k) clearance on 1991-01-28, under 510(k) number K904917.

Who is the listed applicant for THAYER MIP ADAPTER?

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

What is the FDA product code for THAYER MIP ADAPTER?

The FDA product code for THAYER MIP ADAPTER is BXR.

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 Thayer Medical 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 15 devices →

Related Devices (Code: BXR)

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.

↑