VALLEY FORGE BIPOLAR PEN OR FORCEPS
K-Number: K910510 · 1991-04-22
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Device Summary
Frequently Asked Questions
What is the VALLEY FORGE BIPOLAR PEN OR FORCEPS?
VALLEY FORGE BIPOLAR PEN OR FORCEPS is a medical device that received FDA 510(k) clearance on 1991-04-22. The listed applicant is Valley Forge Scientific Corp.. The 510(k) number is K910510.
When did VALLEY FORGE BIPOLAR PEN OR FORCEPS receive FDA 510(k) clearance?
VALLEY FORGE BIPOLAR PEN OR FORCEPS received FDA 510(k) clearance on 1991-04-22, under 510(k) number K910510.
Who is the listed applicant for VALLEY FORGE BIPOLAR PEN OR FORCEPS?
The FDA 510(k) record lists Valley Forge Scientific Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VALLEY FORGE BIPOLAR PEN OR FORCEPS?
The FDA product code for VALLEY FORGE BIPOLAR PEN OR FORCEPS is GEI.
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 Valley Forge Scientific 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.
Related Devices (Code: GEI)
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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