APPARATUS, SUCTION, WARD USE, PORTAB-
K-Number: K843750 · 1984-10-11
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Device Summary
Frequently Asked Questions
What is the APPARATUS, SUCTION, WARD USE, PORTAB-?
APPARATUS, SUCTION, WARD USE, PORTAB- is a medical device that received FDA 510(k) clearance on 1984-10-11. The listed applicant is H.C.H. Products, Inc.. The 510(k) number is K843750.
When did APPARATUS, SUCTION, WARD USE, PORTAB- receive FDA 510(k) clearance?
APPARATUS, SUCTION, WARD USE, PORTAB- received FDA 510(k) clearance on 1984-10-11, under 510(k) number K843750.
Who is the listed applicant for APPARATUS, SUCTION, WARD USE, PORTAB-?
The FDA 510(k) record lists H.C.H. Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for APPARATUS, SUCTION, WARD USE, PORTAB-?
The FDA product code for APPARATUS, SUCTION, WARD USE, PORTAB- is BTA.
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 H.C.H. Products, 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: BTA)
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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