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FDA 510(k)

MICRO-MISTER

K-Number: K903580 · 1990-12-27

ApplicantBp , Ltd.
Decision Date1990-12-27
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MICRO-MISTER is the device name listed in this FDA 510(k) record. The listed applicant is Bp , Ltd.. It received FDA 510(k) clearance on 1990-12-27 under 510(k) number K903580. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-MISTER?

MICRO-MISTER is a medical device that received FDA 510(k) clearance on 1990-12-27. The listed applicant is Bp , Ltd.. The 510(k) number is K903580.

When did MICRO-MISTER receive FDA 510(k) clearance?

MICRO-MISTER received FDA 510(k) clearance on 1990-12-27, under 510(k) number K903580.

Who is the listed applicant for MICRO-MISTER?

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

What is the FDA product code for MICRO-MISTER?

The FDA product code for MICRO-MISTER is CAF.

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 Bp , Ltd. 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.

Related Devices (Code: CAF)

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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