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FDA 510(k)

STERILE CARBON STEEL SURGICAL BLADE

K-Number: K900266 · 1990-03-01

ApplicantRahn Laboratories
Decision Date1990-03-01
Product CodeGES
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERILE CARBON STEEL SURGICAL BLADE is the device name listed in this FDA 510(k) record. The listed applicant is Rahn Laboratories. It received FDA 510(k) clearance on 1990-03-01 under 510(k) number K900266. The device is classified under product code GES. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE CARBON STEEL SURGICAL BLADE?

STERILE CARBON STEEL SURGICAL BLADE is a medical device that received FDA 510(k) clearance on 1990-03-01. The listed applicant is Rahn Laboratories. The 510(k) number is K900266.

When did STERILE CARBON STEEL SURGICAL BLADE receive FDA 510(k) clearance?

STERILE CARBON STEEL SURGICAL BLADE received FDA 510(k) clearance on 1990-03-01, under 510(k) number K900266.

Who is the listed applicant for STERILE CARBON STEEL SURGICAL BLADE?

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

What is the FDA product code for STERILE CARBON STEEL SURGICAL BLADE?

The FDA product code for STERILE CARBON STEEL SURGICAL BLADE is GES.

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 Rahn Laboratories 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.

K892461NON-STERILE LATEX EXAMINATION GLOVESK881479OPERATION ROOM TOWEL

Related Devices (Code: GES)

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.

K032242PERSONNA PLUS SAFETY SCALPEL SYSTEMOmi Manufacturing Pty., Ltd.K932998EASY-ONDevon Industries, Inc.K923170LOS ALAMOS RETRACTABLE KNIFEInnovative Surgical Technology, Inc.K915119SCALPEL BLADE REMOVER (BLADEGARD)Intergrated Visual, Inc.K911913PRECISION GLIDE - ENHANCED SURGICAL BLADEBd Becton Dickinson Vacutainer Systems PreanalyticK884862ANCHOR DOUBLE-EDGE MYRINGOTOMY BLADEAnchor Products Co.

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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