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FDA 510(k)

STANDARD PECTORALIS MUSCLE IMPLANT

K-Number: K790245 · 1979-04-04

ApplicantMedical Engineering Corp.
Decision Date1979-04-04
Product Code
DecisionSubstantially Equivalent

Device Summary

STANDARD PECTORALIS MUSCLE IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Medical Engineering Corp.. It received FDA 510(k) clearance on 1979-04-04 under 510(k) number K790245. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STANDARD PECTORALIS MUSCLE IMPLANT?

STANDARD PECTORALIS MUSCLE IMPLANT is a medical device that received FDA 510(k) clearance on 1979-04-04. The listed applicant is Medical Engineering Corp.. The 510(k) number is K790245.

When did STANDARD PECTORALIS MUSCLE IMPLANT receive FDA 510(k) clearance?

STANDARD PECTORALIS MUSCLE IMPLANT received FDA 510(k) clearance on 1979-04-04, under 510(k) number K790245.

Who is the listed applicant for STANDARD PECTORALIS MUSCLE IMPLANT?

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

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Other records listing Medical Engineering Corp. as applicant

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.

K934141STAND ALONE CYSTOMETROGRAMK905289SURGITEK(R) LUBRI-FLEX(TM) URETERAL STENTK903448SURGITEK TEX-SPAN TEXTURED TISSUE EXPANDERK902773SURGITEK(R) FLEXIBLE URETEROSCOPY INTRO/SHEATH SETK884746SURGITEK FLAT T-SPANK883274SURGITEK (R) UROFLOW SYSTEM

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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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