BEDPAN, SINGLE PATIENT USE, TECNOL
K-Number: K760307 · 1976-08-11
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Device Summary
Frequently Asked Questions
What is the BEDPAN, SINGLE PATIENT USE, TECNOL?
BEDPAN, SINGLE PATIENT USE, TECNOL is a medical device that received FDA 510(k) clearance on 1976-08-11. The listed applicant is Tecnol New Jersey Wound Care, Inc.. The 510(k) number is K760307.
When did BEDPAN, SINGLE PATIENT USE, TECNOL receive FDA 510(k) clearance?
BEDPAN, SINGLE PATIENT USE, TECNOL received FDA 510(k) clearance on 1976-08-11, under 510(k) number K760307.
Who is the listed applicant for BEDPAN, SINGLE PATIENT USE, TECNOL?
The FDA 510(k) record lists Tecnol New Jersey Wound Care, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BEDPAN, SINGLE PATIENT USE, TECNOL?
The FDA product code for BEDPAN, SINGLE PATIENT USE, TECNOL is FOB.
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 Tecnol New Jersey Wound Care, Inc. 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: FOB)
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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