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FDA 510(k)

ET-RESTRAINT CAT. # ER 4000

K-Number: K900236 · 1990-02-02

ApplicantVentlab Corp.
Decision Date1990-02-02
Product CodeCBH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ET-RESTRAINT CAT. # ER 4000 is the device name listed in this FDA 510(k) record. The listed applicant is Ventlab Corp.. It received FDA 510(k) clearance on 1990-02-02 under 510(k) number K900236. The device is classified under product code CBH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ET-RESTRAINT CAT. # ER 4000?

ET-RESTRAINT CAT. # ER 4000 is a medical device that received FDA 510(k) clearance on 1990-02-02. The listed applicant is Ventlab Corp.. The 510(k) number is K900236.

When did ET-RESTRAINT CAT. # ER 4000 receive FDA 510(k) clearance?

ET-RESTRAINT CAT. # ER 4000 received FDA 510(k) clearance on 1990-02-02, under 510(k) number K900236.

Who is the listed applicant for ET-RESTRAINT CAT. # ER 4000?

The FDA 510(k) record lists Ventlab Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ET-RESTRAINT CAT. # ER 4000?

The FDA product code for ET-RESTRAINT CAT. # ER 4000 is CBH.

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Other records listing Ventlab Corp. 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.

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Related Devices (Code: CBH)

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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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