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FDA 510(k)

HOSPAL MODEL H1210

K-Number: K840814 · 1984-04-02

ApplicantHospal Medical Corp.
Decision Date1984-04-02
Product CodeFKQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HOSPAL MODEL H1210 is the device name listed in this FDA 510(k) record. The listed applicant is Hospal Medical Corp.. It received FDA 510(k) clearance on 1984-04-02 under 510(k) number K840814. The device is classified under product code FKQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOSPAL MODEL H1210?

HOSPAL MODEL H1210 is a medical device that received FDA 510(k) clearance on 1984-04-02. The listed applicant is Hospal Medical Corp.. The 510(k) number is K840814.

When did HOSPAL MODEL H1210 receive FDA 510(k) clearance?

HOSPAL MODEL H1210 received FDA 510(k) clearance on 1984-04-02, under 510(k) number K840814.

Who is the listed applicant for HOSPAL MODEL H1210?

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

What is the FDA product code for HOSPAL MODEL H1210?

The FDA product code for HOSPAL MODEL H1210 is FKQ.

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Other records listing Hospal Medical Corp. as applicant

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Related Devices (Code: FKQ)

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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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