MODELS MR700/MR720/MR730 DUAL SERVO RESP HUMID ACC
K-Number: K913368 · 1992-01-13
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Device Summary
Frequently Asked Questions
What is the MODELS MR700/MR720/MR730 DUAL SERVO RESP HUMID ACC?
MODELS MR700/MR720/MR730 DUAL SERVO RESP HUMID ACC is a medical device that received FDA 510(k) clearance on 1992-01-13. The listed applicant is Fisher & Paykel Electronics , Ltd.. The 510(k) number is K913368.
When did MODELS MR700/MR720/MR730 DUAL SERVO RESP HUMID ACC receive FDA 510(k) clearance?
MODELS MR700/MR720/MR730 DUAL SERVO RESP HUMID ACC received FDA 510(k) clearance on 1992-01-13, under 510(k) number K913368.
Who is the listed applicant for MODELS MR700/MR720/MR730 DUAL SERVO RESP HUMID ACC?
The FDA 510(k) record lists Fisher & Paykel Electronics , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODELS MR700/MR720/MR730 DUAL SERVO RESP HUMID ACC?
The FDA product code for MODELS MR700/MR720/MR730 DUAL SERVO RESP HUMID ACC is BTT.
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 Fisher & Paykel Electronics , Ltd. 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: BTT)
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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