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FDA 510(k)

FRANK INHALER THERMAL S

K-Number: K895115 · 1990-05-18

ApplicantButtner-Frank GmbH
Decision Date1990-05-18
Product CodeCCQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FRANK INHALER THERMAL S is the device name listed in this FDA 510(k) record. The listed applicant is Buttner-Frank GmbH. It received FDA 510(k) clearance on 1990-05-18 under 510(k) number K895115. 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 FRANK INHALER THERMAL S?

FRANK INHALER THERMAL S is a medical device that received FDA 510(k) clearance on 1990-05-18. The listed applicant is Buttner-Frank GmbH. The 510(k) number is K895115.

When did FRANK INHALER THERMAL S receive FDA 510(k) clearance?

FRANK INHALER THERMAL S received FDA 510(k) clearance on 1990-05-18, under 510(k) number K895115.

Who is the listed applicant for FRANK INHALER THERMAL S?

The FDA 510(k) record lists Buttner-Frank GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FRANK INHALER THERMAL S?

The FDA product code for FRANK INHALER THERMAL S is CCQ.

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 Buttner-Frank GmbH 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.

K895114FRANK MILK PUMP

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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