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FDA 510(k)

MASS SPECTROMETER-MEDSPECT II

K-Number: K810938 · 1981-04-23

Decision Date1981-04-23
Product CodeDOP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MASS SPECTROMETER-MEDSPECT II is the device name listed in this FDA 510(k) record. The listed applicant is Allied Healthcare Products, Inc.. It received FDA 510(k) clearance on 1981-04-23 under 510(k) number K810938. The device is classified under product code DOP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MASS SPECTROMETER-MEDSPECT II?

MASS SPECTROMETER-MEDSPECT II is a medical device that received FDA 510(k) clearance on 1981-04-23. The listed applicant is Allied Healthcare Products, Inc.. The 510(k) number is K810938.

When did MASS SPECTROMETER-MEDSPECT II receive FDA 510(k) clearance?

MASS SPECTROMETER-MEDSPECT II received FDA 510(k) clearance on 1981-04-23, under 510(k) number K810938.

Who is the listed applicant for MASS SPECTROMETER-MEDSPECT II?

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

What is the FDA product code for MASS SPECTROMETER-MEDSPECT II?

The FDA product code for MASS SPECTROMETER-MEDSPECT II is DOP.

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.

Other records listing Allied Healthcare Products, 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.

View all 24 devices →

Related Devices (Code: DOP)

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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