BARRIER PLASTIC PACKAGING (MODIFICATION)
K-Number: K933560 · 1994-04-11
Advertisement
Device Summary
Frequently Asked Questions
What is the BARRIER PLASTIC PACKAGING (MODIFICATION)?
BARRIER PLASTIC PACKAGING (MODIFICATION) is a medical device that received FDA 510(k) clearance on 1994-04-11. The listed applicant is Maxxim Medical. The 510(k) number is K933560.
When did BARRIER PLASTIC PACKAGING (MODIFICATION) receive FDA 510(k) clearance?
BARRIER PLASTIC PACKAGING (MODIFICATION) received FDA 510(k) clearance on 1994-04-11, under 510(k) number K933560.
Who is the listed applicant for BARRIER PLASTIC PACKAGING (MODIFICATION)?
The FDA 510(k) record lists Maxxim Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BARRIER PLASTIC PACKAGING (MODIFICATION)?
The FDA product code for BARRIER PLASTIC PACKAGING (MODIFICATION) is KCT.
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 Maxxim Medical 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: KCT)
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.
Advertisement