HUNTLEIGH DOUBLE BUBBLE AIR-O-PAD-AOP5
K-Number: K882644 · 1988-08-10
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Device Summary
Frequently Asked Questions
What is the HUNTLEIGH DOUBLE BUBBLE AIR-O-PAD-AOP5?
HUNTLEIGH DOUBLE BUBBLE AIR-O-PAD-AOP5 is a medical device that received FDA 510(k) clearance on 1988-08-10. The listed applicant is Huntleigh Technology, Inc.. The 510(k) number is K882644.
When did HUNTLEIGH DOUBLE BUBBLE AIR-O-PAD-AOP5 receive FDA 510(k) clearance?
HUNTLEIGH DOUBLE BUBBLE AIR-O-PAD-AOP5 received FDA 510(k) clearance on 1988-08-10, under 510(k) number K882644.
Who is the listed applicant for HUNTLEIGH DOUBLE BUBBLE AIR-O-PAD-AOP5?
The FDA 510(k) record lists Huntleigh Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HUNTLEIGH DOUBLE BUBBLE AIR-O-PAD-AOP5?
The FDA product code for HUNTLEIGH DOUBLE BUBBLE AIR-O-PAD-AOP5 is FNM.
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 Huntleigh Technology, 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: FNM)
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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