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FDA 510(k)

ANNULAR ARRAY PROBES FOR ARTIS 3200 DIAG. ULTRA.

K-Number: K881185 · 1988-06-01

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1988-06-01
Product CodeHEM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ANNULAR ARRAY PROBES FOR ARTIS 3200 DIAG. ULTRA. is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems (Cleveland), Inc.. It received FDA 510(k) clearance on 1988-06-01 under 510(k) number K881185. The device is classified under product code HEM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANNULAR ARRAY PROBES FOR ARTIS 3200 DIAG. ULTRA.?

ANNULAR ARRAY PROBES FOR ARTIS 3200 DIAG. ULTRA. is a medical device that received FDA 510(k) clearance on 1988-06-01. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K881185.

When did ANNULAR ARRAY PROBES FOR ARTIS 3200 DIAG. ULTRA. receive FDA 510(k) clearance?

ANNULAR ARRAY PROBES FOR ARTIS 3200 DIAG. ULTRA. received FDA 510(k) clearance on 1988-06-01, under 510(k) number K881185.

Who is the listed applicant for ANNULAR ARRAY PROBES FOR ARTIS 3200 DIAG. ULTRA.?

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

What is the FDA product code for ANNULAR ARRAY PROBES FOR ARTIS 3200 DIAG. ULTRA.?

The FDA product code for ANNULAR ARRAY PROBES FOR ARTIS 3200 DIAG. ULTRA. is HEM.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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