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FDA 510(k)

HAKOMED ELECDT/VACUPULLS

K-Number: K980958 · 1998-05-11

ApplicantAlive, Inc.
Decision Date1998-05-11
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HAKOMED ELECDT/VACUPULLS is the device name listed in this FDA 510(k) record. The listed applicant is Alive, Inc.. It received FDA 510(k) clearance on 1998-05-11 under 510(k) number K980958. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAKOMED ELECDT/VACUPULLS?

HAKOMED ELECDT/VACUPULLS is a medical device that received FDA 510(k) clearance on 1998-05-11. The listed applicant is Alive, Inc.. The 510(k) number is K980958.

When did HAKOMED ELECDT/VACUPULLS receive FDA 510(k) clearance?

HAKOMED ELECDT/VACUPULLS received FDA 510(k) clearance on 1998-05-11, under 510(k) number K980958.

Who is the listed applicant for HAKOMED ELECDT/VACUPULLS?

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

What is the FDA product code for HAKOMED ELECDT/VACUPULLS?

The FDA product code for HAKOMED ELECDT/VACUPULLS is IPF.

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Other records listing Alive, 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.

K980892HAKOMED ELECDT / PRO ELEDT SERIES

Related Devices (Code: IPF)

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.

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Official Source

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