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FDA 510(k)

RETRACTOR, GERBODE STERNAL

K-Number: K760650 · 1976-09-21

ApplicantDilling Co.
Decision Date1976-09-21
Product CodeGAP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RETRACTOR, GERBODE STERNAL is the device name listed in this FDA 510(k) record. The listed applicant is Dilling Co.. It received FDA 510(k) clearance on 1976-09-21 under 510(k) number K760650. The device is classified under product code GAP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RETRACTOR, GERBODE STERNAL?

RETRACTOR, GERBODE STERNAL is a medical device that received FDA 510(k) clearance on 1976-09-21. The listed applicant is Dilling Co.. The 510(k) number is K760650.

When did RETRACTOR, GERBODE STERNAL receive FDA 510(k) clearance?

RETRACTOR, GERBODE STERNAL received FDA 510(k) clearance on 1976-09-21, under 510(k) number K760650.

Who is the listed applicant for RETRACTOR, GERBODE STERNAL?

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

What is the FDA product code for RETRACTOR, GERBODE STERNAL?

The FDA product code for RETRACTOR, GERBODE STERNAL is GAP.

Related Clinical Trials

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.

Related Devices (Code: GAP)

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.

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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