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FDA 510(k)

ADVANCED MICRO-OSMOMETER MODEL 3300

K-Number: K962056 · 1996-07-11

Decision Date1996-07-11
Product CodeJJM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ADVANCED MICRO-OSMOMETER MODEL 3300 is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Instruments, Inc.. It received FDA 510(k) clearance on 1996-07-11 under 510(k) number K962056. The device is classified under product code JJM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVANCED MICRO-OSMOMETER MODEL 3300?

ADVANCED MICRO-OSMOMETER MODEL 3300 is a medical device that received FDA 510(k) clearance on 1996-07-11. The listed applicant is Advanced Instruments, Inc.. The 510(k) number is K962056.

When did ADVANCED MICRO-OSMOMETER MODEL 3300 receive FDA 510(k) clearance?

ADVANCED MICRO-OSMOMETER MODEL 3300 received FDA 510(k) clearance on 1996-07-11, under 510(k) number K962056.

Who is the listed applicant for ADVANCED MICRO-OSMOMETER MODEL 3300?

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

What is the FDA product code for ADVANCED MICRO-OSMOMETER MODEL 3300?

The FDA product code for ADVANCED MICRO-OSMOMETER MODEL 3300 is JJM.

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 Advanced Instruments, 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.

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Related Devices (Code: JJM)

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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