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FDA 510(k)

ADAPTER-STRAIGHT

K-Number: K790564 · 1979-04-12

ApplicantDlp, Inc.
Decision Date1979-04-12
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ADAPTER-STRAIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Dlp, Inc.. It received FDA 510(k) clearance on 1979-04-12 under 510(k) number K790564. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADAPTER-STRAIGHT?

ADAPTER-STRAIGHT is a medical device that received FDA 510(k) clearance on 1979-04-12. The listed applicant is Dlp, Inc.. The 510(k) number is K790564.

When did ADAPTER-STRAIGHT receive FDA 510(k) clearance?

ADAPTER-STRAIGHT received FDA 510(k) clearance on 1979-04-12, under 510(k) number K790564.

Who is the listed applicant for ADAPTER-STRAIGHT?

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

What is the FDA product code for ADAPTER-STRAIGHT?

The FDA product code for ADAPTER-STRAIGHT is DTL.

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Other records listing Dlp, Inc. as applicant

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Related Devices (Code: DTL)

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

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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