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FDA 510(k)

PUMP VAC PLUS

K-Number: K910907 · 1991-05-13

Decision Date1991-05-13
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PUMP VAC PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Marlo Surgical Technology. It received FDA 510(k) clearance on 1991-05-13 under 510(k) number K910907. 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 PUMP VAC PLUS?

PUMP VAC PLUS is a medical device that received FDA 510(k) clearance on 1991-05-13. The listed applicant is Marlo Surgical Technology. The 510(k) number is K910907.

When did PUMP VAC PLUS receive FDA 510(k) clearance?

PUMP VAC PLUS received FDA 510(k) clearance on 1991-05-13, under 510(k) number K910907.

Who is the listed applicant for PUMP VAC PLUS?

The FDA 510(k) record lists Marlo Surgical Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PUMP VAC PLUS?

The FDA product code for PUMP VAC PLUS is HET.

Other records listing Marlo Surgical Technology 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 28 devices →

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

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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