SIMS INTERTECH HYPERINFLATION BAG SYSTEM
K-Number: K952214 · 1995-06-08
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Device Summary
Frequently Asked Questions
What is the SIMS INTERTECH HYPERINFLATION BAG SYSTEM?
SIMS INTERTECH HYPERINFLATION BAG SYSTEM is a medical device that received FDA 510(k) clearance on 1995-06-08. The listed applicant is Intertech Resources, Inc.. The 510(k) number is K952214.
When did SIMS INTERTECH HYPERINFLATION BAG SYSTEM receive FDA 510(k) clearance?
SIMS INTERTECH HYPERINFLATION BAG SYSTEM received FDA 510(k) clearance on 1995-06-08, under 510(k) number K952214.
Who is the listed applicant for SIMS INTERTECH HYPERINFLATION BAG SYSTEM?
The FDA 510(k) record lists Intertech Resources, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SIMS INTERTECH HYPERINFLATION BAG SYSTEM?
The FDA product code for SIMS INTERTECH HYPERINFLATION BAG SYSTEM is NHK.
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 Intertech Resources, 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: NHK)
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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