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FDA 510(k)

COLLINS CPL

K-Number: K992743 · 1999-09-13

ApplicantCollins Medical, Inc.
Decision Date1999-09-13
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

COLLINS CPL is the device name listed in this FDA 510(k) record. The listed applicant is Collins Medical, Inc.. It received FDA 510(k) clearance on 1999-09-13 under 510(k) number K992743. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLLINS CPL?

COLLINS CPL is a medical device that received FDA 510(k) clearance on 1999-09-13. The listed applicant is Collins Medical, Inc.. The 510(k) number is K992743.

When did COLLINS CPL receive FDA 510(k) clearance?

COLLINS CPL received FDA 510(k) clearance on 1999-09-13, under 510(k) number K992743.

Who is the listed applicant for COLLINS CPL?

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

What is the FDA product code for COLLINS CPL?

The FDA product code for COLLINS CPL is BZG.

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.

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Other records listing Collins Medical, 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.

K030917GEM; HAWK; EAGLE; MODELS 004110, 0044120, 004130K030464GEM, MODEL 004110K011344INFANT PLETHYSMOGRAPH, MODEL 004400; PEDIATRIC PLETHYSMOGRAPH, MODEL 004400

Related Devices (Code: BZG)

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.

K251777MESI mTABLET SPIROMesi D.O.O.K241843TD-7301 Spirometer (TD-7301)Gostar Co., Ltd.K231416Air Next (NVD-02)Nuvoair ABK230501Spirobank OxiMir Medical International Research USAK230178EasyOne Sky SpirometerNdd Medizintechnik AGK222525Alveoair Digital SpirometerRoundworks Technologies Private Limited

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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