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FDA 510(k)

BEAR CUB 750 PSV

K-Number: K992788 · 1999-09-16

Decision Date1999-09-16
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BEAR CUB 750 PSV is the device name listed in this FDA 510(k) record. The listed applicant is Bear Medical Systems, Inc.. It received FDA 510(k) clearance on 1999-09-16 under 510(k) number K992788. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEAR CUB 750 PSV?

BEAR CUB 750 PSV is a medical device that received FDA 510(k) clearance on 1999-09-16. The listed applicant is Bear Medical Systems, Inc.. The 510(k) number is K992788.

When did BEAR CUB 750 PSV receive FDA 510(k) clearance?

BEAR CUB 750 PSV received FDA 510(k) clearance on 1999-09-16, under 510(k) number K992788.

Who is the listed applicant for BEAR CUB 750 PSV?

The FDA 510(k) record lists Bear Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BEAR CUB 750 PSV?

The FDA product code for BEAR CUB 750 PSV is CBK.

Other records listing Bear Medical Systems, 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.

View all 28 devices →

Related Devices (Code: CBK)

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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