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FDA 510(k)

AQUAHAB, MODEL 120-72-101

K-Number: K945733 · 1995-09-15

ApplicantAquarius Electronics, Inc.
Decision Date1995-09-15
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

AQUAHAB, MODEL 120-72-101 is the device name listed in this FDA 510(k) record. The listed applicant is Aquarius Electronics, Inc.. It received FDA 510(k) clearance on 1995-09-15 under 510(k) number K945733. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AQUAHAB, MODEL 120-72-101?

AQUAHAB, MODEL 120-72-101 is a medical device that received FDA 510(k) clearance on 1995-09-15. The listed applicant is Aquarius Electronics, Inc.. The 510(k) number is K945733.

When did AQUAHAB, MODEL 120-72-101 receive FDA 510(k) clearance?

AQUAHAB, MODEL 120-72-101 received FDA 510(k) clearance on 1995-09-15, under 510(k) number K945733.

Who is the listed applicant for AQUAHAB, MODEL 120-72-101?

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

What is the FDA product code for AQUAHAB, MODEL 120-72-101?

The FDA product code for AQUAHAB, MODEL 120-72-101 is BXB.

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Related Devices (Code: BXB)

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

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