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FDA 510(k)

SAFE-T-TUBE RADIOPAQUE

K-Number: K930150 · 1993-02-12

Decision Date1993-02-12
Product CodeBTR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SAFE-T-TUBE RADIOPAQUE is the device name listed in this FDA 510(k) record. The listed applicant is Boston Medical Products, Inc.. It received FDA 510(k) clearance on 1993-02-12 under 510(k) number K930150. The device is classified under product code BTR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAFE-T-TUBE RADIOPAQUE?

SAFE-T-TUBE RADIOPAQUE is a medical device that received FDA 510(k) clearance on 1993-02-12. The listed applicant is Boston Medical Products, Inc.. The 510(k) number is K930150.

When did SAFE-T-TUBE RADIOPAQUE receive FDA 510(k) clearance?

SAFE-T-TUBE RADIOPAQUE received FDA 510(k) clearance on 1993-02-12, under 510(k) number K930150.

Who is the listed applicant for SAFE-T-TUBE RADIOPAQUE?

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

What is the FDA product code for SAFE-T-TUBE RADIOPAQUE?

The FDA product code for SAFE-T-TUBE RADIOPAQUE is BTR.

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 Boston Medical Products, 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.

View all 33 devices →

Related Devices (Code: BTR)

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.

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