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FDA 510(k)

BEDPAN, SINGLE PATIENT USE, TECNOL

K-Number: K760307 · 1976-08-11

Decision Date1976-08-11
Product CodeFOB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BEDPAN, SINGLE PATIENT USE, TECNOL is the device name listed in this FDA 510(k) record. The listed applicant is Tecnol New Jersey Wound Care, Inc.. It received FDA 510(k) clearance on 1976-08-11 under 510(k) number K760307. The device is classified under product code FOB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 35 devices →

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

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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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