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FDA 510(k)

SUCTION AND LAVAGE PROBE

K-Number: K874614 · 1988-06-23

Decision Date1988-06-23
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SUCTION AND LAVAGE PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Marketing, Inc.. It received FDA 510(k) clearance on 1988-06-23 under 510(k) number K874614. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUCTION AND LAVAGE PROBE?

SUCTION AND LAVAGE PROBE is a medical device that received FDA 510(k) clearance on 1988-06-23. The listed applicant is Medical Marketing, Inc.. The 510(k) number is K874614.

When did SUCTION AND LAVAGE PROBE receive FDA 510(k) clearance?

SUCTION AND LAVAGE PROBE received FDA 510(k) clearance on 1988-06-23, under 510(k) number K874614.

Who is the listed applicant for SUCTION AND LAVAGE PROBE?

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

What is the FDA product code for SUCTION AND LAVAGE PROBE?

The FDA product code for SUCTION AND LAVAGE PROBE is HET.

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 Medical Marketing, 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.

Related Devices (Code: HET)

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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