PREFILLED NEBULIZER — Corpak Co. (510(k) K810218)

Name: PREFILLED NEBULIZER — Corpak Co. (510(k) K810218)
Creator: DeviceClear

PREFILLED NEBULIZER — Corpak Co. (510(k) K810218) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: PREFILLED NEBULIZER; Applicant: Corpak Co.; Clearance track: 510(k).

Device name	PREFILLED NEBULIZER
Applicant	Corpak Co.
Clearance track	510(k)
Submission number	K810218
Decision	Substantially Equivalent
Decision date	1981-03-04
Date received	1981-01-27
Product code	CAF
Device class	2
Medical specialty	Anesthesiology
Applicant location	IL, US
Source	openFDA device

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$1999/mo

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