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FDA 510(k)

THUMB DRESSING FORCEPS 5

K-Number: K821282 · 1982-05-28

ApplicantConphar, Inc.
Decision Date1982-05-28
Product CodeEFL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

THUMB DRESSING FORCEPS 5 is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1982-05-28 under 510(k) number K821282. The device is classified under product code EFL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THUMB DRESSING FORCEPS 5?

THUMB DRESSING FORCEPS 5 is a medical device that received FDA 510(k) clearance on 1982-05-28. The listed applicant is Conphar, Inc.. The 510(k) number is K821282.

When did THUMB DRESSING FORCEPS 5 receive FDA 510(k) clearance?

THUMB DRESSING FORCEPS 5 received FDA 510(k) clearance on 1982-05-28, under 510(k) number K821282.

Who is the listed applicant for THUMB DRESSING FORCEPS 5?

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

What is the FDA product code for THUMB DRESSING FORCEPS 5?

The FDA product code for THUMB DRESSING FORCEPS 5 is EFL.

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 Conphar, 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 122 devices →

Related Devices (Code: EFL)

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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