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FDA 510(k)

CARE-E-VAC

K-Number: K926566 · 1993-07-09

Decision Date1993-07-09
Product CodeBTA
Advisory CommitteeSU
DecisionUnknown

Device Summary

CARE-E-VAC is the device name listed in this FDA 510(k) record. The listed applicant is Aeros Instruments, Inc.. It received FDA 510(k) clearance on 1993-07-09 under 510(k) number K926566. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CARE-E-VAC?

CARE-E-VAC is a medical device that received FDA 510(k) clearance on 1993-07-09. The listed applicant is Aeros Instruments, Inc.. The 510(k) number is K926566.

When did CARE-E-VAC receive FDA 510(k) clearance?

CARE-E-VAC received FDA 510(k) clearance on 1993-07-09, under 510(k) number K926566.

Who is the listed applicant for CARE-E-VAC?

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

What is the FDA product code for CARE-E-VAC?

The FDA product code for CARE-E-VAC is BTA.

Other records listing Aeros Instruments, 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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