MEDI-MIST PORTA. COMPRESSOR DRIVEN
K-Number: K833501 · 1983-12-12
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Device Summary
Frequently Asked Questions
What is the MEDI-MIST PORTA. COMPRESSOR DRIVEN?
MEDI-MIST PORTA. COMPRESSOR DRIVEN is a medical device that received FDA 510(k) clearance on 1983-12-12. The listed applicant is Mountain Medical Equipment, Inc.. The 510(k) number is K833501.
When did MEDI-MIST PORTA. COMPRESSOR DRIVEN receive FDA 510(k) clearance?
MEDI-MIST PORTA. COMPRESSOR DRIVEN received FDA 510(k) clearance on 1983-12-12, under 510(k) number K833501.
Who is the listed applicant for MEDI-MIST PORTA. COMPRESSOR DRIVEN?
The FDA 510(k) record lists Mountain Medical Equipment, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDI-MIST PORTA. COMPRESSOR DRIVEN?
The FDA product code for MEDI-MIST PORTA. COMPRESSOR DRIVEN is BTI.
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 Mountain Medical Equipment, 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: BTI)
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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