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FDA 510(k)

PRE-DUCED SURGI-SWAB & TRANSPORTER TUBE

K-Number: K761241 · 1976-12-30

ApplicantGibco Laboratories Life Technologies, Inc.
Decision Date1976-12-30
Product CodeJTX
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PRE-DUCED SURGI-SWAB & TRANSPORTER TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Gibco Laboratories Life Technologies, Inc.. It received FDA 510(k) clearance on 1976-12-30 under 510(k) number K761241. The device is classified under product code JTX. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRE-DUCED SURGI-SWAB & TRANSPORTER TUBE?

PRE-DUCED SURGI-SWAB & TRANSPORTER TUBE is a medical device that received FDA 510(k) clearance on 1976-12-30. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K761241.

When did PRE-DUCED SURGI-SWAB & TRANSPORTER TUBE receive FDA 510(k) clearance?

PRE-DUCED SURGI-SWAB & TRANSPORTER TUBE received FDA 510(k) clearance on 1976-12-30, under 510(k) number K761241.

Who is the listed applicant for PRE-DUCED SURGI-SWAB & TRANSPORTER TUBE?

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

What is the FDA product code for PRE-DUCED SURGI-SWAB & TRANSPORTER TUBE?

The FDA product code for PRE-DUCED SURGI-SWAB & TRANSPORTER TUBE is JTX.

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Other records listing Gibco Laboratories Life Technologies, Inc. as applicant

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K871855SORBITOL MACCONKEY (SMAC) AGAR, DRI & PRE-FORMK871541MARTIN-LEWIS AGAR W/REDUCED VANCOMYCIN C0226K870134MCBRIDE LISTERIA AGAR W/CYCLOHEXIMIDE, DRI & PREK864755PSEUDOMONAS CEPACIA SELECTIVE AGAR, DRI & PRE-FORMK864014LOMBARD DOWELL AGAR BASEK863821MUELLER HINTON AGAR W/4%NACL AND OXACILLIN

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Related Devices (Code: JTX)

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.

K901645ANAEROBIC ACCU-CULSHURE(TM)Medical Laboratory Automation Systems, Inc.K897151ACUSON V328 AND C5432 TRANSDUCERSAcuson Corp.K882637ACCU-CULSHURE TMAccu-Med Corp.K791724BIO-BAG ENVIRONMENTAL CHAMBER (A & B)Marion Laboratories, Inc.K781376STANDARDIZE TGCL & TGCHAmerican Monitor Corp.K780159ANASWABScott Laboratories, Inc.

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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