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FDA 510(k)

CALIBRATED BREATHING SYSTEM COLLECTION

K-Number: K811955 · 1981-08-04

Decision Date1981-08-04
Product CodeKDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CALIBRATED BREATHING SYSTEM COLLECTION is the device name listed in this FDA 510(k) record. The listed applicant is Anchor Brush Co., Inc.. It received FDA 510(k) clearance on 1981-08-04 under 510(k) number K811955. The device is classified under product code KDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CALIBRATED BREATHING SYSTEM COLLECTION?

CALIBRATED BREATHING SYSTEM COLLECTION is a medical device that received FDA 510(k) clearance on 1981-08-04. The listed applicant is Anchor Brush Co., Inc.. The 510(k) number is K811955.

When did CALIBRATED BREATHING SYSTEM COLLECTION receive FDA 510(k) clearance?

CALIBRATED BREATHING SYSTEM COLLECTION received FDA 510(k) clearance on 1981-08-04, under 510(k) number K811955.

Who is the listed applicant for CALIBRATED BREATHING SYSTEM COLLECTION?

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

What is the FDA product code for CALIBRATED BREATHING SYSTEM COLLECTION?

The FDA product code for CALIBRATED BREATHING SYSTEM COLLECTION is KDQ.

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.

Related Devices (Code: KDQ)

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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