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FDA 510(k)

MODELS DPT 1000/DPT 1000NS

K-Number: K823286 · 1982-12-30

ApplicantBio-Med Corp.
Decision Date1982-12-30
Product CodeDRS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODELS DPT 1000/DPT 1000NS is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Med Corp.. It received FDA 510(k) clearance on 1982-12-30 under 510(k) number K823286. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODELS DPT 1000/DPT 1000NS?

MODELS DPT 1000/DPT 1000NS is a medical device that received FDA 510(k) clearance on 1982-12-30. The listed applicant is Bio-Med Corp.. The 510(k) number is K823286.

When did MODELS DPT 1000/DPT 1000NS receive FDA 510(k) clearance?

MODELS DPT 1000/DPT 1000NS received FDA 510(k) clearance on 1982-12-30, under 510(k) number K823286.

Who is the listed applicant for MODELS DPT 1000/DPT 1000NS?

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

What is the FDA product code for MODELS DPT 1000/DPT 1000NS?

The FDA product code for MODELS DPT 1000/DPT 1000NS is DRS.

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Other records listing Bio-Med Corp. as applicant

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Related Devices (Code: DRS)

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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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