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FDA 510(k)

SERACON -LO DO26

K-Number: K791957 · 1979-10-11

ApplicantBhp Diagnostix, Inc.
Decision Date1979-10-11
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SERACON -LO DO26 is the device name listed in this FDA 510(k) record. The listed applicant is Bhp Diagnostix, Inc.. It received FDA 510(k) clearance on 1979-10-11 under 510(k) number K791957. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERACON -LO DO26?

SERACON -LO DO26 is a medical device that received FDA 510(k) clearance on 1979-10-11. The listed applicant is Bhp Diagnostix, Inc.. The 510(k) number is K791957.

When did SERACON -LO DO26 receive FDA 510(k) clearance?

SERACON -LO DO26 received FDA 510(k) clearance on 1979-10-11, under 510(k) number K791957.

Who is the listed applicant for SERACON -LO DO26?

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

What is the FDA product code for SERACON -LO DO26?

The FDA product code for SERACON -LO DO26 is JJX.

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Other records listing Bhp Diagnostix, Inc. as applicant

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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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