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FDA 510(k)

GP3%SP-2100DOHON100/120 MESH SUPELCOPORT

K-Number: K761226 · 1977-01-14

ApplicantSupelco, Inc.
Decision Date1977-01-14
Product CodeJSQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GP3%SP-2100DOHON100/120 MESH SUPELCOPORT is the device name listed in this FDA 510(k) record. The listed applicant is Supelco, Inc.. It received FDA 510(k) clearance on 1977-01-14 under 510(k) number K761226. The device is classified under product code JSQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GP3%SP-2100DOHON100/120 MESH SUPELCOPORT?

GP3%SP-2100DOHON100/120 MESH SUPELCOPORT is a medical device that received FDA 510(k) clearance on 1977-01-14. The listed applicant is Supelco, Inc.. The 510(k) number is K761226.

When did GP3%SP-2100DOHON100/120 MESH SUPELCOPORT receive FDA 510(k) clearance?

GP3%SP-2100DOHON100/120 MESH SUPELCOPORT received FDA 510(k) clearance on 1977-01-14, under 510(k) number K761226.

Who is the listed applicant for GP3%SP-2100DOHON100/120 MESH SUPELCOPORT?

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

What is the FDA product code for GP3%SP-2100DOHON100/120 MESH SUPELCOPORT?

The FDA product code for GP3%SP-2100DOHON100/120 MESH SUPELCOPORT is JSQ.

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Other records listing Supelco, Inc. as applicant

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Related Devices (Code: JSQ)

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.

K834007CYSTINE TRYPTIC MEDIUMMicro Media LaboratoriesK811138NUTRIENT AGARAcumedia Manufacturers, 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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