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FDA 510(k)

TRIANGULAR JAW MICROLARYNGEAL FORCEPS

K-Number: K925370 · 1993-03-18

ApplicantPilling Co.
Decision Date1993-03-18
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TRIANGULAR JAW MICROLARYNGEAL FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1993-03-18 under 510(k) number K925370. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIANGULAR JAW MICROLARYNGEAL FORCEPS?

TRIANGULAR JAW MICROLARYNGEAL FORCEPS is a medical device that received FDA 510(k) clearance on 1993-03-18. The listed applicant is Pilling Co.. The 510(k) number is K925370.

When did TRIANGULAR JAW MICROLARYNGEAL FORCEPS receive FDA 510(k) clearance?

TRIANGULAR JAW MICROLARYNGEAL FORCEPS received FDA 510(k) clearance on 1993-03-18, under 510(k) number K925370.

Who is the listed applicant for TRIANGULAR JAW MICROLARYNGEAL FORCEPS?

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

What is the FDA product code for TRIANGULAR JAW MICROLARYNGEAL FORCEPS?

The FDA product code for TRIANGULAR JAW MICROLARYNGEAL FORCEPS is ELW.

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.

Other records listing Pilling Co. 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.

View all 39 devices →

Related Devices (Code: ELW)

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

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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