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FDA 510(k)

STAPLE REMOVER SR300P

K-Number: K833085 · 1984-12-14

ApplicantProsper, Inc.
Decision Date1984-12-14
Product CodeGDT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STAPLE REMOVER SR300P is the device name listed in this FDA 510(k) record. The listed applicant is Prosper, Inc.. It received FDA 510(k) clearance on 1984-12-14 under 510(k) number K833085. The device is classified under product code GDT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAPLE REMOVER SR300P?

STAPLE REMOVER SR300P is a medical device that received FDA 510(k) clearance on 1984-12-14. The listed applicant is Prosper, Inc.. The 510(k) number is K833085.

When did STAPLE REMOVER SR300P receive FDA 510(k) clearance?

STAPLE REMOVER SR300P received FDA 510(k) clearance on 1984-12-14, under 510(k) number K833085.

Who is the listed applicant for STAPLE REMOVER SR300P?

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

What is the FDA product code for STAPLE REMOVER SR300P?

The FDA product code for STAPLE REMOVER SR300P is GDT.

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.

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Other records listing Prosper, 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.

K832709SKIN STAPLING DEVICE SC2000

Related Devices (Code: GDT)

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.

K963234STAPLE REMOVAL KITContinental Medical Laboratories, Inc.K943719VISISTAT STAPLERPilling Weck, Inc.K925526MANIPLER DISPOSABLE SKIN STAPLERMatsutani Seisakusho Co. , Ltd.K915430SKIN STAPLE REMOVER KITCypress Medical Products, Ltd.K911204QUALTEX SKIN STAPLE EXTRACTORDeroyal Industries, Inc.K910586AUTO SUTURE(R) POLYMER SKIN GRAFT STAPLER*United States Surgical, A Division of Tyco Healthc

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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