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FDA 510(k)

COMMUNI-CALL

K-Number: K893473 · 1989-06-09

Decision Date1989-06-09
Product CodeILQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

COMMUNI-CALL is the device name listed in this FDA 510(k) record. The listed applicant is Carepartners, Inc.. It received FDA 510(k) clearance on 1989-06-09 under 510(k) number K893473. The device is classified under product code ILQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMMUNI-CALL?

COMMUNI-CALL is a medical device that received FDA 510(k) clearance on 1989-06-09. The listed applicant is Carepartners, Inc.. The 510(k) number is K893473.

When did COMMUNI-CALL receive FDA 510(k) clearance?

COMMUNI-CALL received FDA 510(k) clearance on 1989-06-09, under 510(k) number K893473.

Who is the listed applicant for COMMUNI-CALL?

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

What is the FDA product code for COMMUNI-CALL?

The FDA product code for COMMUNI-CALL is ILQ.

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.

Related Devices (Code: ILQ)

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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