BIOBOX TRAPTOP (SMALL, MEDIUM, LARGE AND X-LARGE)
K-Number: K950897 · 1995-08-24
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Device Summary
Frequently Asked Questions
What is the BIOBOX TRAPTOP (SMALL, MEDIUM, LARGE AND X-LARGE)?
BIOBOX TRAPTOP (SMALL, MEDIUM, LARGE AND X-LARGE) is a medical device that received FDA 510(k) clearance on 1995-08-24. The listed applicant is Biosystems. The 510(k) number is K950897.
When did BIOBOX TRAPTOP (SMALL, MEDIUM, LARGE AND X-LARGE) receive FDA 510(k) clearance?
BIOBOX TRAPTOP (SMALL, MEDIUM, LARGE AND X-LARGE) received FDA 510(k) clearance on 1995-08-24, under 510(k) number K950897.
Who is the listed applicant for BIOBOX TRAPTOP (SMALL, MEDIUM, LARGE AND X-LARGE)?
The FDA 510(k) record lists Biosystems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIOBOX TRAPTOP (SMALL, MEDIUM, LARGE AND X-LARGE)?
The FDA product code for BIOBOX TRAPTOP (SMALL, MEDIUM, LARGE AND X-LARGE) is MMK.
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 Biosystems 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: MMK)
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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