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FDA 510(k)

CROUP TENT FRAME

K-Number: K842192 · 1984-06-25

ApplicantHome Run Treadmill Co.
Decision Date1984-06-25
Product CodeCCQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CROUP TENT FRAME is the device name listed in this FDA 510(k) record. The listed applicant is Home Run Treadmill Co.. It received FDA 510(k) clearance on 1984-06-25 under 510(k) number K842192. The device is classified under product code CCQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CROUP TENT FRAME?

CROUP TENT FRAME is a medical device that received FDA 510(k) clearance on 1984-06-25. The listed applicant is Home Run Treadmill Co.. The 510(k) number is K842192.

When did CROUP TENT FRAME receive FDA 510(k) clearance?

CROUP TENT FRAME received FDA 510(k) clearance on 1984-06-25, under 510(k) number K842192.

Who is the listed applicant for CROUP TENT FRAME?

The FDA 510(k) record lists Home Run Treadmill Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CROUP TENT FRAME?

The FDA product code for CROUP TENT FRAME is CCQ.

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Related Devices (Code: CCQ)

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.

K972397EZ SPRAYIntertex Research, Inc.K964956E-Z SPACER MASK (SMALL)Airpharma, LLCK961894MDI TUTORMdi Tutor, Inc.K961455MEDSHIELD/AEROCHAMBERDiemolding Corp.K960593SMARTMIST ASTHMA MANAGMENT SYSTEM, SMARTMIST, MODEL NUMBER SM-100/SMARTMIST SPIROMETRY AIRWAY, MODEL NUMBER SA-100Aradigm Corp.K922033SALINE SOLUTION- STERILETrinity Laboratories, Inc.

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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