MONTGOMERY SAFE-T-TUBE
K-Number: K843936 · 1984-12-14
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Device Summary
Frequently Asked Questions
What is the MONTGOMERY SAFE-T-TUBE?
MONTGOMERY SAFE-T-TUBE is a medical device that received FDA 510(k) clearance on 1984-12-14. The listed applicant is Boston Medical Products, Inc.. The 510(k) number is K843936.
When did MONTGOMERY SAFE-T-TUBE receive FDA 510(k) clearance?
MONTGOMERY SAFE-T-TUBE received FDA 510(k) clearance on 1984-12-14, under 510(k) number K843936.
Who is the listed applicant for MONTGOMERY SAFE-T-TUBE?
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 MONTGOMERY SAFE-T-TUBE?
The FDA product code for MONTGOMERY SAFE-T-TUBE 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.
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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