BEMIS STERILE-CASE FOR USE W/ETHYLENE OXIDE STERI.
K-Number: K885019 · 1989-01-25
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Device Summary
Frequently Asked Questions
What is the BEMIS STERILE-CASE FOR USE W/ETHYLENE OXIDE STERI.?
BEMIS STERILE-CASE FOR USE W/ETHYLENE OXIDE STERI. is a medical device that received FDA 510(k) clearance on 1989-01-25. The listed applicant is Bemis Health Care. The 510(k) number is K885019.
When did BEMIS STERILE-CASE FOR USE W/ETHYLENE OXIDE STERI. receive FDA 510(k) clearance?
BEMIS STERILE-CASE FOR USE W/ETHYLENE OXIDE STERI. received FDA 510(k) clearance on 1989-01-25, under 510(k) number K885019.
Who is the listed applicant for BEMIS STERILE-CASE FOR USE W/ETHYLENE OXIDE STERI.?
The FDA 510(k) record lists Bemis Health Care as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BEMIS STERILE-CASE FOR USE W/ETHYLENE OXIDE STERI.?
The FDA product code for BEMIS STERILE-CASE FOR USE W/ETHYLENE OXIDE STERI. is FRG.
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 Bemis Health Care 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: FRG)
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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