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FDA 510(k)

FORCEPS, MOSQUITO STYLE, 12.5 CM.

K-Number: K770540 · 1977-04-15

Decision Date1977-04-15
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FORCEPS, MOSQUITO STYLE, 12.5 CM. is the device name listed in this FDA 510(k) record. The listed applicant is Sea-Pac Trading Corp.. It received FDA 510(k) clearance on 1977-04-15 under 510(k) number K770540. The device is classified under product code GEN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORCEPS, MOSQUITO STYLE, 12.5 CM.?

FORCEPS, MOSQUITO STYLE, 12.5 CM. is a medical device that received FDA 510(k) clearance on 1977-04-15. The listed applicant is Sea-Pac Trading Corp.. The 510(k) number is K770540.

When did FORCEPS, MOSQUITO STYLE, 12.5 CM. receive FDA 510(k) clearance?

FORCEPS, MOSQUITO STYLE, 12.5 CM. received FDA 510(k) clearance on 1977-04-15, under 510(k) number K770540.

Who is the listed applicant for FORCEPS, MOSQUITO STYLE, 12.5 CM.?

The FDA 510(k) record lists Sea-Pac Trading Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FORCEPS, MOSQUITO STYLE, 12.5 CM.?

The FDA product code for FORCEPS, MOSQUITO STYLE, 12.5 CM. is GEN.

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 Sea-Pac Trading Corp. 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 7 devices →

Related Devices (Code: GEN)

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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