CHAMBER, MC-1 DISPOSABLE PRESSURE
K-Number: K781890 · 1978-12-04
Advertisement
Device Summary
Frequently Asked Questions
What is the CHAMBER, MC-1 DISPOSABLE PRESSURE?
CHAMBER, MC-1 DISPOSABLE PRESSURE is a medical device that received FDA 510(k) clearance on 1978-12-04. The listed applicant is Delta Medical Industries. The 510(k) number is K781890.
When did CHAMBER, MC-1 DISPOSABLE PRESSURE receive FDA 510(k) clearance?
CHAMBER, MC-1 DISPOSABLE PRESSURE received FDA 510(k) clearance on 1978-12-04, under 510(k) number K781890.
Who is the listed applicant for CHAMBER, MC-1 DISPOSABLE PRESSURE?
The FDA 510(k) record lists Delta Medical Industries as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CHAMBER, MC-1 DISPOSABLE PRESSURE?
The FDA product code for CHAMBER, MC-1 DISPOSABLE PRESSURE is DXS.
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 Delta Medical Industries 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: DXS)
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.
Advertisement