BOTTLE-TO-BOTTLE
K-Number: K811268 · 1981-06-18
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Device Summary
Frequently Asked Questions
What is the BOTTLE-TO-BOTTLE?
BOTTLE-TO-BOTTLE is a medical device that received FDA 510(k) clearance on 1981-06-18. The listed applicant is Medi-Plast Intl., Inc.. The 510(k) number is K811268.
When did BOTTLE-TO-BOTTLE receive FDA 510(k) clearance?
BOTTLE-TO-BOTTLE received FDA 510(k) clearance on 1981-06-18, under 510(k) number K811268.
Who is the listed applicant for BOTTLE-TO-BOTTLE?
The FDA 510(k) record lists Medi-Plast Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BOTTLE-TO-BOTTLE?
The FDA product code for BOTTLE-TO-BOTTLE is KPE.
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 Medi-Plast Intl., 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: KPE)
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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