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FDA 510(k)

PACIFIC COMMUNICATIONS MODEL 1100

K-Number: K942147 · 1995-01-30

Decision Date1995-01-30
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PACIFIC COMMUNICATIONS MODEL 1100 is the device name listed in this FDA 510(k) record. The listed applicant is Accucore, Inc.. It received FDA 510(k) clearance on 1995-01-30 under 510(k) number K942147. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PACIFIC COMMUNICATIONS MODEL 1100?

PACIFIC COMMUNICATIONS MODEL 1100 is a medical device that received FDA 510(k) clearance on 1995-01-30. The listed applicant is Accucore, Inc.. The 510(k) number is K942147.

When did PACIFIC COMMUNICATIONS MODEL 1100 receive FDA 510(k) clearance?

PACIFIC COMMUNICATIONS MODEL 1100 received FDA 510(k) clearance on 1995-01-30, under 510(k) number K942147.

Who is the listed applicant for PACIFIC COMMUNICATIONS MODEL 1100?

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

What is the FDA product code for PACIFIC COMMUNICATIONS MODEL 1100?

The FDA product code for PACIFIC COMMUNICATIONS MODEL 1100 is DSI.

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 Accucore, 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 9 devices →

Related Devices (Code: DSI)

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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