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FDA 510(k)

KALLESTAD R QUANTIPLATE ALT. PATHWAY T.

K-Number: K811445 · 1981-06-24

ApplicantKallestad Laboratories, Inc.
Decision Date1981-06-24
Product CodeDHL
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

KALLESTAD R QUANTIPLATE ALT. PATHWAY T. is the device name listed in this FDA 510(k) record. The listed applicant is Kallestad Laboratories, Inc.. It received FDA 510(k) clearance on 1981-06-24 under 510(k) number K811445. The device is classified under product code DHL. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KALLESTAD R QUANTIPLATE ALT. PATHWAY T.?

KALLESTAD R QUANTIPLATE ALT. PATHWAY T. is a medical device that received FDA 510(k) clearance on 1981-06-24. The listed applicant is Kallestad Laboratories, Inc.. The 510(k) number is K811445.

When did KALLESTAD R QUANTIPLATE ALT. PATHWAY T. receive FDA 510(k) clearance?

KALLESTAD R QUANTIPLATE ALT. PATHWAY T. received FDA 510(k) clearance on 1981-06-24, under 510(k) number K811445.

Who is the listed applicant for KALLESTAD R QUANTIPLATE ALT. PATHWAY T.?

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

What is the FDA product code for KALLESTAD R QUANTIPLATE ALT. PATHWAY T.?

The FDA product code for KALLESTAD R QUANTIPLATE ALT. PATHWAY T. is DHL.

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Related Devices (Code: DHL)

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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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